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PedAM

Pediatric Disease Annotations & Medicines



   hydrocephalus
  

Disease ID 180
Disease hydrocephalus
Definition
Excessive accumulation of cerebrospinal fluid within the cranium which may be associated with dilation of cerebral ventricles, INTRACRANIAL HYPERTENSION; HEADACHE; lethargy; URINARY INCONTINENCE; and ATAXIA.
Synonym
hydrencephalus
hydrencephaly
hydrocephalus (disorder)
hydrocephalus [disease/finding]
hydrocephaly
nonsyndromal hydrocephalus
water on the brain
OMIM
DOID
UMLS
C0020255
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:126)
C0025289  |  meningitis  |  28
C0041318  |  tuberculous meningitis  |  14
C0151740  |  increased intracranial pressure  |  12
C0151740  |  intracranial hypertension  |  10
C0080178  |  spina bifida  |  8
C0020538  |  hypertension  |  7
C0151740  |  raised intracranial pressure  |  6
C0078981  |  arachnoid cyst  |  6
C0041318  |  tubercular meningitis  |  5
C0221355  |  macrocephaly  |  5
C0036202  |  sarcoidosis  |  4
C0039144  |  syringomyelia  |  3
C0037198  |  sinus thrombosis  |  3
C0025149  |  medulloblastoma  |  3
C0010964  |  dandy-walker malformation  |  3
C0151740  |  elevated intracranial pressure  |  3
C0010278  |  craniosynostosis  |  3
C0007785  |  cerebral infarct  |  3
C0027809  |  schwannoma  |  2
C0162429  |  malnourished  |  2
C0154653  |  chronic meningitis  |  2
C0014544  |  epilepsy  |  2
C0029124  |  optic atrophy  |  2
C0027859  |  vestibular schwannomas  |  2
C0027859  |  vestibular schwannoma  |  2
C0002395  |  alzheimer's disease  |  2
C0078981  |  arachnoid cysts  |  2
C0026709  |  mps vi  |  2
C0085437  |  bacterial meningitis  |  2
C0917996  |  cerebral aneurysm  |  2
C0007785  |  cerebral infarction  |  2
C0151860  |  porencephaly  |  2
C0001080  |  achondroplasia  |  2
C0010276  |  craniopharyngioma  |  2
C0040558  |  toxoplasmosis  |  2
C0013384  |  dyskinesia  |  2
C0007766  |  intracranial aneurysm  |  2
C0497327  |  dementia  |  2
C0155285  |  orbital cyst  |  2
C0040053  |  thrombosis  |  2
C0007766  |  cranial aneurysm  |  2
C0018378  |  guillain-barre syndrome  |  1
C1527390  |  intracranial tumors  |  1
C0006111  |  brain disorders  |  1
C0338451  |  frontotemporal dementia  |  1
C0553662  |  juvenile ra  |  1
C0026780  |  mumps  |  1
C0027859  |  acoustic neuroma  |  1
C0026703  |  mucopolysaccharidosis  |  1
C0024523  |  malabsorption  |  1
C0011649  |  dermoid cyst  |  1
C0018916  |  hemangioma  |  1
C0029401  |  paget's disease  |  1
C0007785  |  cerebral infarcts  |  1
C0025309  |  meningoencephalitis  |  1
C0028945  |  oligodendroglioma  |  1
C0023521  |  krabbe disease  |  1
C0035309  |  retinal disease  |  1
C0041296  |  tuberculosis  |  1
C0003857  |  arteriovenous malformation  |  1
C0270639  |  lateral sinus thrombosis  |  1
C0206620  |  hygroma  |  1
C0027873  |  neuromyelitis optica  |  1
C0205898  |  pineoblastoma  |  1
C0085404  |  poems syndrome  |  1
C0020635  |  hypopituitarism  |  1
C0205770  |  choroid plexus papilloma  |  1
C0020258  |  normal pressure hydrocephalus  |  1
C0027859  |  acoustic neuromas  |  1
C0011649  |  dermoid  |  1
C1862179  |  cerebellar medulloblastoma  |  1
C0879615  |  stromal tumor  |  1
C0426970  |  spastic quadriplegia  |  1
C0007789  |  cerebral palsy  |  1
C0085273  |  parvovirus b19 infection  |  1
C0012569  |  diplopia  |  1
C0025149  |  medulloblastomas  |  1
C0026934  |  mycoplasma  |  1
C0031154  |  peritonitis  |  1
C0021400  |  influenza  |  1
C0026850  |  muscular dystrophy  |  1
C0026709  |  mucopolysaccharidosis type vi  |  1
C0003873  |  rheumatoid arthritis  |  1
C0524851  |  neurodegenerative disorders  |  1
C0334583  |  pilocytic astrocytoma  |  1
C0085315  |  cns toxoplasmosis  |  1
C0032285  |  pneumoniae  |  1
C1704231  |  leptomeningeal metastasis  |  1
C0009241  |  cognitive disorders  |  1
C0010273  |  crouzon syndrome  |  1
C0080178  |  spinal dysraphism  |  1
C0018931  |  hematocele  |  1
C0018213  |  graves' disease  |  1
C1334271  |  intraventricular meningioma  |  1
C0006111  |  brain disorder  |  1
C0085220  |  cerebral amyloid angiopathy  |  1
C0679466  |  cognitive deficits  |  1
C0003466  |  imperforate anus  |  1
C0752347  |  dementia with lewy bodies  |  1
C0025362  |  mental retardation  |  1
C0220650  |  brain metastases  |  1
C0028326  |  noonan syndrome  |  1
C0043092  |  wegener's granulomatosis  |  1
C0686377  |  cns metastasis  |  1
C0085113  |  neurofibromatosis  |  1
C0265343  |  jarcho-levin syndrome  |  1
C0002395  |  alzheimer disease  |  1
C0010273  |  crouzon's syndrome  |  1
C0039538  |  teratoma  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0268583  |  methylmalonic aciduria  |  1
C0017205  |  gaucher disease  |  1
C0004114  |  astrocytoma  |  1
C0266463  |  lissencephaly  |  1
C0041341  |  phacomatosis  |  1
C1332900  |  cerebellar hemangioblastoma  |  1
C0206734  |  hemangioblastoma  |  1
C0032000  |  pituitary adenoma  |  1
C0238198  |  gastrointestinal stromal tumor  |  1
C0338575  |  sagittal sinus thrombosis  |  1
C0022116  |  ischaemia  |  1
C0008780  |  primary ciliary dyskinesia  |  1
C1704231  |  leptomeningeal metastases  |  1
C1527390  |  intracranial tumor  |  1
C0032285  |  pneumonia  |  1
C0027858  |  neuromas  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
IFT122  |  55764  |  CTD_human
HYDIN  |  54768  |  CTD_human
THAS  |  7055  |  CTD_human
CCDC88C  |  440193  |  CLINVAR
ISPD  |  729920  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
1636  |  ACE  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:479)
10301  |  DLEU1  |  DISEASES
2288  |  FKBP4  |  DISEASES
2519  |  FUCA2  |  DISEASES
1634  |  DCN  |  DISEASES
90956  |  ADCK2  |  DISEASES
23152  |  CIC  |  DISEASES
1951  |  CELSR3  |  DISEASES
57595  |  PDZD4  |  DISEASES
27248  |  ERLEC1  |  DISEASES
8646  |  CHRD  |  DISEASES
57106  |  NAT14  |  DISEASES
3162  |  HMOX1  |  DISEASES
5020  |  OXT  |  DISEASES
123876  |  ACSM2A  |  DISEASES
79152  |  FA2H  |  DISEASES
7249  |  TSC2  |  DISEASES
7783  |  ZP2  |  DISEASES
1445  |  CSK  |  DISEASES
51285  |  RASL12  |  DISEASES
5327  |  PLAT  |  DISEASES
333  |  APLP1  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
1406  |  CRX  |  DISEASES
5296  |  PIK3R2  |  DISEASES
3696  |  ITGB8  |  DISEASES
3199  |  HOXA2  |  DISEASES
8976  |  WASL  |  DISEASES
2218  |  FKTN  |  DISEASES
7448  |  VTN  |  DISEASES
24145  |  PANX1  |  DISEASES
5250  |  SLC25A3  |  DISEASES
2026  |  ENO2  |  DISEASES
1432  |  MAPK14  |  DISEASES
150465  |  TTL  |  DISEASES
10153  |  CEBPZ  |  DISEASES
7276  |  TTR  |  DISEASES
5311  |  PKD2  |  DISEASES
84417  |  C2orf40  |  DISEASES
55640  |  FLVCR2  |  DISEASES
7043  |  TGFB3  |  DISEASES
4488  |  MSX2  |  DISEASES
7976  |  FZD3  |  DISEASES
10804  |  GJB6  |  DISEASES
2700  |  GJA3  |  DISEASES
4852  |  NPY  |  DISEASES
7291  |  TWIST1  |  DISEASES
6718  |  AKR1D1  |  DISEASES
4035  |  LRP1  |  DISEASES
8358  |  HIST1H3B  |  DISEASES
79143  |  MBOAT7  |  DISEASES
2354  |  FOSB  |  DISEASES
1340  |  COX6B1  |  DISEASES
22879  |  MON1B  |  DISEASES
14  |  AAMP  |  DISEASES
23639  |  LRRC6  |  DISEASES
9509  |  ADAMTS2  |  DISEASES
348  |  APOE  |  DISEASES
1463  |  NCAN  |  DISEASES
10343  |  PKDREJ  |  DISEASES
2670  |  GFAP  |  DISEASES
56033  |  BARX1  |  DISEASES
85415  |  RHPN2  |  DISEASES
6538  |  SLC6A11  |  DISEASES
3021  |  H3F3B  |  DISEASES
1401  |  CRP  |  DISEASES
10752  |  CHL1  |  DISEASES
129607  |  CMPK2  |  DISEASES
3569  |  IL6  |  DISEASES
4836  |  NMT1  |  DISEASES
6496  |  SIX3  |  DISEASES
23314  |  SATB2  |  DISEASES
3417  |  IDH1  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
10329  |  TMEM5  |  DISEASES
9786  |  KIAA0586  |  DISEASES
2581  |  GALC  |  DISEASES
29954  |  POMT2  |  DISEASES
64398  |  MPP5  |  DISEASES
10961  |  ERP29  |  DISEASES
55697  |  VAC14  |  DISEASES
5689  |  PSMB1  |  DISEASES
4591  |  TRIM37  |  DISEASES
5310  |  PKD1  |  DISEASES
1770  |  DNAH9  |  DISEASES
6132  |  RPL8  |  DISEASES
9368  |  SLC9A3R1  |  DISEASES
6845  |  VAMP7  |  DISEASES
9620  |  CELSR1  |  DISEASES
25939  |  SAMHD1  |  DISEASES
5050  |  PAFAH1B3  |  DISEASES
10133  |  OPTN  |  DISEASES
6598  |  SMARCB1  |  DISEASES
421  |  ARVCF  |  DISEASES
6855  |  SYP  |  DISEASES
2033  |  EP300  |  DISEASES
3553  |  IL1B  |  DISEASES
8775  |  NAPA  |  DISEASES
10000  |  AKT3  |  DISEASES
390  |  RND3  |  DISEASES
84708  |  LNX1  |  DISEASES
5290  |  PIK3CA  |  DISEASES
56912  |  IFT46  |  DISEASES
2743  |  GLRB  |  DISEASES
2247  |  FGF2  |  DISEASES
5443  |  POMC  |  DISEASES
411  |  ARSB  |  DISEASES
2121  |  EVC  |  DISEASES
1767  |  DNAH5  |  DISEASES
8382  |  NME5  |  DISEASES
793  |  CALB1  |  DISEASES
10312  |  TCIRG1  |  DISEASES
54443  |  ANLN  |  DISEASES
8034  |  SLC25A16  |  DISEASES
25809  |  TTLL1  |  DISEASES
8620  |  NPFF  |  DISEASES
122481  |  AK7  |  DISEASES
1000  |  CDH2  |  DISEASES
7157  |  TP53  |  DISEASES
126374  |  WTIP  |  DISEASES
6531  |  SLC6A3  |  DISEASES
1952  |  CELSR2  |  DISEASES
163859  |  SDE2  |  DISEASES
285362  |  SUMF1  |  DISEASES
4841  |  NONO  |  DISEASES
23196  |  FAM120A  |  DISEASES
4851  |  NOTCH1  |  DISEASES
6768  |  ST14  |  DISEASES
22897  |  CEP164  |  DISEASES
9871  |  SEC24D  |  DISEASES
23657  |  SLC7A11  |  DISEASES
3948  |  LDHC  |  DISEASES
288  |  ANK3  |  DISEASES
132320  |  SCLT1  |  DISEASES
5458  |  POU4F2  |  DISEASES
7082  |  TJP1  |  DISEASES
2895  |  GRID2  |  DISEASES
26040  |  SETBP1  |  DISEASES
6695  |  SPOCK1  |  DISEASES
10309  |  CCNO  |  DISEASES
170692  |  ADAMTS18  |  DISEASES
1360  |  CPB1  |  DISEASES
6317  |  SERPINB3  |  DISEASES
351  |  APP  |  DISEASES
760  |  CA2  |  DISEASES
4838  |  NODAL  |  DISEASES
7547  |  ZIC3  |  DISEASES
6750  |  SST  |  DISEASES
7079  |  TIMP4  |  DISEASES
57477  |  SHROOM4  |  DISEASES
168507  |  PKD1L1  |  DISEASES
6285  |  S100B  |  DISEASES
7471  |  WNT1  |  DISEASES
362  |  AQP5  |  DISEASES
4880  |  NPPC  |  DISEASES
27148  |  STK36  |  DISEASES
23380  |  SRGAP2  |  DISEASES
213  |  ALB  |  DISEASES
166336  |  PRICKLE2  |  DISEASES
56979  |  PRDM9  |  DISEASES
6469  |  SHH  |  DISEASES
55582  |  KIF27  |  DISEASES
364  |  AQP7  |  DISEASES
360  |  AQP3  |  DISEASES
83550  |  GPR101  |  DISEASES
55172  |  DNAAF2  |  DISEASES
158067  |  AK8  |  DISEASES
79841  |  AGBL2  |  DISEASES
9317  |  PTER  |  DISEASES
7846  |  TUBA1A  |  DISEASES
80150  |  ASRGL1  |  DISEASES
54986  |  ULK4  |  DISEASES
5617  |  PRL  |  DISEASES
79058  |  ASPSCR1  |  DISEASES
116844  |  LRG1  |  DISEASES
3479  |  IGF1  |  DISEASES
153241  |  CEP120  |  DISEASES
8988  |  HSPB3  |  DISEASES
29  |  ABR  |  DISEASES
260434  |  PYDC1  |  DISEASES
340024  |  SLC6A19  |  DISEASES
4968  |  OGG1  |  DISEASES
1473  |  CST5  |  DISEASES
794  |  CALB2  |  DISEASES
10886  |  NPFFR2  |  DISEASES
197259  |  MLKL  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
29925  |  GMPPB  |  DISEASES
947  |  CD34  |  DISEASES
23209  |  MLC1  |  DISEASES
392  |  ARHGAP1  |  DISEASES
358  |  AQP1  |  DISEASES
11007  |  CCDC85B  |  DISEASES
1605  |  DAG1  |  DISEASES
55885  |  LMO3  |  DISEASES
666  |  BOK  |  DISEASES
998  |  CDC42  |  DISEASES
54768  |  HYDIN  |  DISEASES
64231  |  MS4A6A  |  DISEASES
55690  |  PACS1  |  DISEASES
582  |  BBS1  |  DISEASES
4762  |  NEUROG1  |  DISEASES
4684  |  NCAM1  |  DISEASES
282679  |  AQP11  |  DISEASES
84231  |  TRAF7  |  DISEASES
137814  |  NKX2-6  |  DISEASES
7182  |  NR2C2  |  DISEASES
8289  |  ARID1A  |  DISEASES
161582  |  DYX1C1  |  DISEASES
8100  |  IFT88  |  DISEASES
2302  |  FOXJ1  |  DISEASES
2200  |  FBN1  |  DISEASES
60626  |  RIC8A  |  DISEASES
113457  |  TUBA3D  |  DISEASES
5663  |  PSEN1  |  DISEASES
2303  |  FOXC2  |  DISEASES
79147  |  FKRP  |  DISEASES
2187  |  FANCB  |  DISEASES
5108  |  PCM1  |  DISEASES
8905  |  AP1S2  |  DISEASES
125061  |  AFMID  |  DISEASES
8354  |  HIST1H3I  |  DISEASES
6900  |  CNTN2  |  DISEASES
10215  |  OLIG2  |  DISEASES
63827  |  BCAN  |  DISEASES
5136  |  PDE1A  |  DISEASES
83482  |  SCRT1  |  DISEASES
5727  |  PTCH1  |  DISEASES
113179  |  ADAT3  |  DISEASES
79582  |  SPAG16  |  DISEASES
145282  |  MIPOL1  |  DISEASES
9001  |  HAP1  |  DISEASES
55742  |  PARVA  |  DISEASES
2152  |  F3  |  DISEASES
2009  |  EML1  |  DISEASES
27445  |  PCLO  |  DISEASES
6887  |  TAL2  |  DISEASES
3842  |  TNPO1  |  DISEASES
1641  |  DCX  |  DISEASES
135138  |  PACRG  |  DISEASES
554  |  AVPR2  |  DISEASES
23583  |  SMUG1  |  DISEASES
8835  |  SOCS2  |  DISEASES
3423  |  IDS  |  DISEASES
2261  |  FGFR3  |  DISEASES
126432  |  RINL  |  DISEASES
10612  |  TRIM3  |  DISEASES
4137  |  MAPT  |  DISEASES
4882  |  NPR2  |  DISEASES
113675  |  SDSL  |  DISEASES
122809  |  SOCS4  |  DISEASES
55274  |  PHF10  |  DISEASES
375567  |  VWC2  |  DISEASES
27255  |  CNTN6  |  DISEASES
10166  |  SLC25A15  |  DISEASES
3198  |  HOXA1  |  DISEASES
29887  |  SNX10  |  DISEASES
5015  |  OTX2  |  DISEASES
5549  |  PRELP  |  DISEASES
53827  |  FXYD5  |  DISEASES
8481  |  OFD1  |  DISEASES
374407  |  DNAJB13  |  DISEASES
4771  |  NF2  |  DISEASES
8326  |  FZD9  |  DISEASES
3921  |  RPSA  |  DISEASES
9719  |  ADAMTSL2  |  DISEASES
4698  |  NDUFA5  |  DISEASES
10438  |  C1D  |  DISEASES
79925  |  SPEF2  |  DISEASES
4649  |  MYO9A  |  DISEASES
219844  |  HYLS1  |  DISEASES
92359  |  CRB3  |  DISEASES
5725  |  PTBP1  |  DISEASES
55691  |  FRMD4A  |  DISEASES
8350  |  HIST1H3A  |  DISEASES
5992  |  RFX4  |  DISEASES
51460  |  SFMBT1  |  DISEASES
4763  |  NF1  |  DISEASES
5294  |  PIK3CG  |  DISEASES
1995  |  ELAVL3  |  DISEASES
10761  |  PLAC1  |  DISEASES
8356  |  HIST1H3J  |  DISEASES
23607  |  CD2AP  |  DISEASES
9220  |  TIAF1  |  DISEASES
79947  |  DHDDS  |  DISEASES
127343  |  DMBX1  |  DISEASES
60509  |  AGBL5  |  DISEASES
2157  |  F8  |  DISEASES
4133  |  MAP2  |  DISEASES
83666  |  PARP9  |  DISEASES
8353  |  HIST1H3E  |  DISEASES
1066  |  CES1  |  DISEASES
10319  |  LAMC3  |  DISEASES
2475  |  MTOR  |  DISEASES
54510  |  PCDH18  |  DISEASES
9444  |  QKI  |  DISEASES
148789  |  B3GALNT2  |  DISEASES
3020  |  H3F3A  |  DISEASES
3142  |  HLX  |  DISEASES
7042  |  TGFB2  |  DISEASES
3664  |  IRF6  |  DISEASES
254428  |  SLC41A1  |  DISEASES
4194  |  MDM4  |  DISEASES
56956  |  LHX9  |  DISEASES
259266  |  ASPM  |  DISEASES
2153  |  F5  |  DISEASES
29922  |  NME7  |  DISEASES
6391  |  SDHC  |  DISEASES
57216  |  VANGL2  |  DISEASES
10763  |  NES  |  DISEASES
81609  |  SNX27  |  DISEASES
7101  |  NR2E1  |  DISEASES
8357  |  HIST1H3H  |  DISEASES
2018  |  EMX2  |  DISEASES
4803  |  NGF  |  DISEASES
128344  |  PIFO  |  DISEASES
257  |  ALX3  |  DISEASES
2316  |  FLNA  |  DISEASES
51684  |  SUFU  |  DISEASES
51750  |  RTEL1  |  DISEASES
393  |  ARHGAP4  |  DISEASES
3897  |  L1CAM  |  DISEASES
25911  |  DPCD  |  DISEASES
1069  |  CETN2  |  DISEASES
6658  |  SOX3  |  DISEASES
959  |  CD40LG  |  DISEASES
2239  |  GPC4  |  DISEASES
4774  |  NFIA  |  DISEASES
7268  |  TTC4  |  DISEASES
1376  |  CPT2  |  DISEASES
5730  |  PTGDS  |  DISEASES
84871  |  AGBL4  |  DISEASES
10564  |  ARFGEF2  |  DISEASES
5728  |  PTEN  |  DISEASES
55624  |  POMGNT1  |  DISEASES
7422  |  VEGFA  |  DISEASES
10585  |  POMT1  |  DISEASES
4318  |  MMP9  |  DISEASES
22845  |  DOLK  |  DISEASES
27286  |  SRPX2  |  DISEASES
55315  |  SLC29A3  |  DISEASES
546  |  ATRX  |  DISEASES
79140  |  CCDC28B  |  DISEASES
286204  |  CRB2  |  DISEASES
2170  |  FABP3  |  DISEASES
84890  |  ADO  |  DISEASES
80114  |  BICC1  |  DISEASES
1269  |  CNR2  |  DISEASES
2159  |  F10  |  DISEASES
22919  |  MAPRE1  |  DISEASES
2155  |  F7  |  DISEASES
1282  |  COL4A1  |  DISEASES
199  |  AIF1  |  DISEASES
4524  |  MTHFR  |  DISEASES
9576  |  SPAG6  |  DISEASES
5394  |  EXOSC10  |  DISEASES
386653  |  IL31  |  DISEASES
10082  |  GPC6  |  DISEASES
81562  |  LMAN2L  |  DISEASES
1910  |  EDNRB  |  DISEASES
8351  |  HIST1H3D  |  DISEASES
57380  |  MRS2  |  DISEASES
51473  |  DCDC2  |  DISEASES
3980  |  LIG3  |  DISEASES
123872  |  DNAAF1  |  DISEASES
11127  |  KIF3A  |  DISEASES
1855  |  DVL1  |  DISEASES
4897  |  NRCAM  |  DISEASES
5080  |  PAX6  |  DISEASES
5212  |  VIT  |  DISEASES
4739  |  NEDD9  |  DISEASES
133482  |  SLCO6A1  |  DISEASES
317762  |  CCDC85C  |  DISEASES
551  |  AVP  |  DISEASES
3045  |  HBD  |  DISEASES
1280  |  COL2A1  |  DISEASES
56897  |  WRNIP1  |  DISEASES
2296  |  FOXC1  |  DISEASES
158326  |  FREM1  |  DISEASES
4781  |  NFIB  |  DISEASES
8777  |  MPDZ  |  DISEASES
3486  |  IGFBP3  |  DISEASES
7054  |  TH  |  DISEASES
2731  |  GLDC  |  DISEASES
51761  |  ATP8A2  |  DISEASES
427  |  ASAH1  |  DISEASES
192668  |  CYS1  |  DISEASES
9751  |  SNPH  |  DISEASES
5991  |  RFX3  |  DISEASES
7436  |  VLDLR  |  DISEASES
26278  |  SACS  |  DISEASES
140850  |  DEFB127  |  DISEASES
4155  |  MBP  |  DISEASES
4487  |  MSX1  |  DISEASES
1186  |  CLCN7  |  DISEASES
3083  |  HGFAC  |  DISEASES
361  |  AQP4  |  DISEASES
9901  |  SRGAP3  |  DISEASES
22908  |  SACM1L  |  DISEASES
10716  |  TBR1  |  DISEASES
8502  |  PKP4  |  DISEASES
440193  |  CCDC88C  |  DISEASES
124602  |  KIF19  |  DISEASES
352909  |  DNAAF3  |  DISEASES
5077  |  PAX3  |  DISEASES
4216  |  MAP3K4  |  DISEASES
9244  |  CRLF1  |  DISEASES
12  |  SERPINA3  |  DISEASES
54903  |  MKS1  |  DISEASES
284076  |  TTLL6  |  DISEASES
5803  |  PTPRZ1  |  DISEASES
200894  |  ARL13B  |  DISEASES
374654  |  KIF7  |  DISEASES
27297  |  CRCP  |  DISEASES
174  |  AFP  |  DISEASES
2737  |  GLI3  |  DISEASES
5048  |  PAFAH1B1  |  DISEASES
4784  |  NFIX  |  DISEASES
594857  |  NPS  |  DISEASES
4905  |  NSF  |  DISEASES
815  |  CAMK2A  |  DISEASES
4644  |  MYO5A  |  DISEASES
1826  |  DSCAM  |  DISEASES
127602  |  DNAH14  |  DISEASES
114800  |  CCDC85A  |  DISEASES
2116  |  ETV2  |  DISEASES
55120  |  FANCL  |  DISEASES
729920  |  ISPD  |  DISEASES
7018  |  TF  |  DISEASES
150737  |  TTC30B  |  DISEASES
93986  |  FOXP2  |  DISEASES
124997  |  WDR81  |  DISEASES
57703  |  CWC22  |  DISEASES
501  |  ALDH7A1  |  DISEASES
176  |  ACAN  |  DISEASES
9048  |  ARTN  |  DISEASES
10640  |  EXOC5  |  DISEASES
3481  |  IGF2  |  DISEASES
5649  |  RELN  |  DISEASES
146713  |  RBFOX3  |  DISEASES
2260  |  FGFR1  |  DISEASES
4125  |  MAN2B1  |  DISEASES
4204  |  MECP2  |  DISEASES
4908  |  NTF3  |  DISEASES
1875  |  E2F5  |  DISEASES
57545  |  CC2D2A  |  DISEASES
5817  |  PVR  |  DISEASES
139728  |  PNCK  |  DISEASES
647309  |  GMNC  |  DISEASES
284252  |  KCTD1  |  DISEASES
2668  |  GDNF  |  DISEASES
2263  |  FGFR2  |  DISEASES
4140  |  MARK3  |  DISEASES
2741  |  GLRA1  |  DISEASES
627  |  BDNF  |  DISEASES
342371  |  ATXN1L  |  DISEASES
5528  |  PPP2R5D  |  DISEASES
79989  |  TTC26  |  DISEASES
9353  |  SLIT2  |  DISEASES
6586  |  SLIT3  |  DISEASES
9152  |  SLC6A5  |  DISEASES
5049  |  PAFAH1B2  |  DISEASES
388015  |  RTL1  |  DISEASES
84107  |  ZIC4  |  DISEASES
55862  |  ECHDC1  |  DISEASES
399687  |  MYO18A  |  DISEASES
8352  |  HIST1H3C  |  DISEASES
8355  |  HIST1H3G  |  DISEASES
51259  |  TMEM216  |  DISEASES
8968  |  HIST1H3F  |  DISEASES
8972  |  MGAM  |  DISEASES
8825  |  LIN7A  |  DISEASES
80184  |  CEP290  |  DISEASES
6642  |  SNX1  |  DISEASES
30837  |  SOCS7  |  DISEASES
4782  |  NFIC  |  DISEASES
102723508  |  KANTR  |  DISEASES
79104  |  MEG8  |  DISEASES
Locus(Waiting for update.)
Disease ID 180
Disease hydrocephalus
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:139)
HP:0001287  |  Meningitis  |  25
HP:0002516  |  Intracranial pressure elevation  |  22
HP:0002664  |  Neoplasia  |  20
HP:0002410  |  Aqueductal stenosis  |  16
HP:0030746  |  Intraventricular hemorrhage  |  10
HP:0002138  |  Subarachnoid hemorrhage  |  9
HP:0000969  |  Dropsy  |  9
HP:0002414  |  Spina bifida  |  8
HP:0002119  |  Ventricular dilatation  |  8
HP:0000822  |  Hypertension  |  7
HP:0002475  |  Myelomeningocele  |  7
HP:0002315  |  Headaches  |  7
HP:0000256  |  Macrocrania  |  7
HP:0045005  |  Neural tube defect  |  6
HP:0002617  |  Aneurysmal dilatation  |  6
HP:0100702  |  Arachnoid cyst  |  6
HP:0100543  |  Cognitive deficits  |  5
HP:0007099  |  Arnold Chiari type I malformation  |  5
HP:0004944  |  Cerebral artery aneurysm  |  4
HP:0030692  |  Brain tumor  |  4
HP:0003396  |  Syringomyelia  |  3
HP:0001268  |  Mental deterioration  |  3
HP:0002308  |  Chiari malformation  |  3
HP:0002885  |  Medulloblastoma  |  3
HP:0011695  |  Cerebellar hemorrhage  |  3
HP:0002170  |  Intracranial hemorrhage  |  3
HP:0001363  |  Early fusion of cranial sutures  |  3
HP:0001305  |  Dandy-Walker cyst  |  3
HP:0009588  |  Vestibular Schwannoma  |  3
HP:0009733  |  Glioma  |  2
HP:0002084  |  Bifid skull  |  2
HP:0002025  |  Narrowing of anal opening  |  2
HP:0001631  |  Atria septal defect  |  2
HP:0000648  |  Optic-nerve degeneration  |  2
HP:0010302  |  Tumor of the spinal cord  |  2
HP:0001144  |  Orbital cysts  |  2
HP:0004936  |  Blood clot in vein  |  2
HP:0100660  |  Dyskinesis  |  2
HP:0001342  |  Intracerebral hemorrhage  |  2
HP:0002132  |  Porencephaly  |  2
HP:0012444  |  Brain wasting  |  2
HP:0030062  |  Craniopharyngioma  |  2
HP:0005305  |  Cerebral vein thrombosis  |  2
HP:0100008  |  Schwann cell tumour  |  2
HP:0001518  |  Small for gestational age  |  2
HP:0003416  |  Spinal canal stenosis  |  2
HP:0002615  |  Low blood pressure  |  2
HP:0002344  |  Progressive neurologic deterioration  |  2
HP:0000726  |  Dementia  |  2
HP:0100310  |  Extradural hematoma  |  1
HP:0100021  |  Cerebral palsy  |  1
HP:0003560  |  Muscular dystrophy  |  1
HP:0002079  |  Hypoplasia of the corpus callosum  |  1
HP:0001254  |  Lethargy  |  1
HP:0012072  |  Aciduria  |  1
HP:0012704  |  Widened subarachnoid space  |  1
HP:0007209  |  Facial paresis  |  1
HP:0030713  |  Vein of Galen malformation  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0012120  |  Methymalonicaciduria  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0003219  |  Ethylmalonic aciduria  |  1
HP:0001320  |  Hypoplasia of the cerebellar vermis  |  1
HP:0001337  |  Tremor  |  1
HP:0040075  |  Hypopituitarism  |  1
HP:0004439  |  Crouzon syndrome  |  1
HP:0001259  |  Coma  |  1
HP:0002181  |  Cerebral edema  |  1
HP:0002145  |  Frontotemporal dementia  |  1
HP:0002024  |  Intestinal malabsorption  |  1
HP:0000020  |  Bladder incontinence  |  1
HP:0006880  |  Hemangioblastoma, sporadic cerebellar  |  1
HP:0010797  |  Hemangioblastoma  |  1
HP:0001278  |  Orthostatic hypotension  |  1
HP:0200022  |  Choroid plexus papilloma  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0001331  |  Agenesis of the septum pellucidum  |  1
HP:0002510  |  Spastic quadriplegia  |  1
HP:0004490  |  Hyperostosis of calvarial bones  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0000078  |  Genital abnormalities  |  1
HP:0004947  |  Arteriovenous fistula  |  1
HP:0007185  |  Loss of consciousness  |  1
HP:0100790  |  Hernia  |  1
HP:0002251  |  Hirschsprung megacolon  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0001289  |  Confusion  |  1
HP:0000568  |  Abnormally small globe of eye  |  1
HP:0002365  |  Hypoplasia of the brainstem  |  1
HP:0002090  |  Pneumonia  |  1
HP:0002085  |  Occipital encephalocele  |  1
HP:0007260  |  Type II lissencephaly  |  1
HP:0010819  |  drop attacks  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0002343  |  Normal-pressure hydrocephalus  |  1
HP:0012265  |  Ciliary dyskinesia  |  1
HP:0001249  |  Mental retardation  |  1
HP:0008936  |  Truncal hypotonia  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0030709  |  Myelocystocele  |  1
HP:0002888  |  Ependymoma  |  1
HP:0011970  |  Cerebral amyloid angiopathy  |  1
HP:0030408  |  Pineoblastoma  |  1
HP:0002072  |  Chorea  |  1
HP:0010524  |  Agnosia  |  1
HP:0002329  |  Drowsiness  |  1
HP:0009792  |  Teratoma  |  1
HP:0001339  |  Lissencephaly  |  1
HP:0008845  |  Mesomelic dwarfism  |  1
HP:0010301  |  Spinal dysraphism  |  1
HP:0012721  |  Venous malformations  |  1
HP:0001321  |  Small cerebellum  |  1
HP:0100723  |  Gastrointestinal stroma tumor  |  1
HP:0007100  |  Progressive ventriculomegaly  |  1
HP:0002511  |  Late-onset form of familial Alzheimer disease  |  1
HP:0100022  |  Movement disorder  |  1
HP:0004322  |  Stature below 3rd percentile  |  1
HP:0001274  |  Absent corpus callosum  |  1
HP:0001288  |  Gait disturbance  |  1
HP:0001362  |  Cranial defect  |  1
HP:0003510  |  Proportionate dwarfism  |  1
HP:0030708  |  Myeloschisis  |  1
HP:0000572  |  Visual loss  |  1
HP:0010880  |  Increased nuchal translucency  |  1
HP:0005306  |  Capillary hemangioma  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0012683  |  Pineal cyst  |  1
HP:0000651  |  Diplopia  |  1
HP:0005857  |  Cervical spina bifida  |  1
HP:0001250  |  Seizures  |  1
HP:0002586  |  Peritonitis  |  1
HP:0002198  |  Enlarged fourth ventricle  |  1
HP:0007129  |  Cerebellar medulloblastoma  |  1
HP:0012027  |  Laryngeal edema  |  1
HP:0001252  |  Hypotonia  |  1
HP:0007033  |  Cerebellar dysplasia  |  1
HP:0000803  |  Cortical cysts  |  1
HP:0009592  |  Astrocytoma  |  1
Disease ID 180
Disease hydrocephalus
Manually Symptom
UMLS  | Name(Total Manually Symptoms:83)
C2707258  |  infections
C2632116  |  stenosis
C2364324  |  increased intracranial pressure
C2096315  |  headache
C2096314  |  facial pain
C2029884  |  hearing loss
C2020541  |  strabismus
C1997217  |  low-grade glioma
C1963138  |  hypertension
C1963101  |  encephalopathy
C1527311  |  brain edema
C1455718  |  ventriculitis
C1442871  |  craniosynostosis
C1421317  |  urofacial syndrome
C1416776  |  congenital muscular dystrophy
C1336049  |  sarcoma of the spinal cord
C1276004  |  bilateral trochlear nerve paresis
C1141920  |  shunt infection
C0854912  |  pineal germinoma
C0796110  |  w syndrome
C0796095  |  c syndrome
C0746408  |  mass lesion
C0547030  |  visual disturbance
C0520731  |  retraction nystagmus
C0497327  |  dementia
C0426768  |  o sign
C0422833  |  ent symptoms
C0346308  |  pituitary macroadenoma
C0340098  |  neurogenic pulmonary edema
C0338591  |  transient global amnesia
C0271885  |  hypothalamic obesity
C0266484  |  schizencephaly
C0265292  |  craniometaphyseal dysplasia
C0264733  |  ventricular dilatation
C0262471  |  ent problem
C0242567  |  opsoclonus
C0242422  |  parkinsonism
C0242422  |  parkinsonian syndromes
C0238074  |  chronic cor pulmonale
C0232940  |  secondary amenorrhea
C0221355  |  macrocephaly
C0206733  |  capillary hemangioma
C0205770  |  choroid plexus papilloma
C0162429  |  undernutrition
C0158534  |  spina bifida
C0152222  |  parinaud's syndrome
C0152134  |  internuclear ophthalmoplegia
C0151740  |  raised intracranial pressure
C0151740  |  intracranial hypertension
C0151740  |  elevated intracranial pressure
C0149931  |  migraine
C0086543  |  cataracts
C0078981  |  arachnoid cyst
C0042928  |  vocal cord paralysis
C0041408  |  turner syndrome
C0039145  |  syringomyelia
C0037939  |  spinal tumors
C0036454  |  visual field defects
C0036454  |  visual field defect
C0030354  |  papilloma
C0030167  |  pachymeningitis
C0027831  |  von recklinghausen's disease
C0027809  |  neurinoma
C0027765  |  neurological disorder
C0026650  |  dyskinesia syndrome
C0025289  |  meningitis
C0024299  |  malignant lymphoma
C0022521  |  immotile cilia syndrome
C0020635  |  hypopituitarism
C0019570  |  hirschsprung's disease
C0018920  |  cavernous hemangioma
C0018681  |  headaches
C0017638  |  gliomas
C0014544  |  epilepsy
C0014306  |  enophthalmos
C0014038  |  encephalitis
C0013604  |  oedema
C0010678  |  cysticercosis
C0010278  |  craniostenosis
C0008780  |  ciliary dyskinesia
C0007815  |  cerebrospinal fluid rhinorrhea
C0007684  |  central nervous system infections
C0006118  |  brain tumors
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:27)
C0025289  |  meningitis  |  25
C0009814  |  stenosis  |  15
C0151740  |  increased intracranial pressure  |  12
C0151740  |  intracranial hypertension  |  10
C0080178  |  spina bifida  |  8
C0020538  |  hypertension  |  7
C0078981  |  arachnoid cyst  |  6
C0151740  |  raised intracranial pressure  |  6
C0018681  |  headache  |  5
C0221355  |  macrocephaly  |  5
C0302598  |  ventriculitis  |  4
C0017638  |  gliomas  |  3
C0039144  |  syringomyelia  |  3
C0151740  |  elevated intracranial pressure  |  3
C0013604  |  oedema  |  3
C0010278  |  craniosynostosis  |  3
C0018681  |  headaches  |  2
C1141920  |  shunt infection  |  2
C0264733  |  ventricular dilatation  |  2
C0497327  |  dementia  |  2
C0426768  |  o sign  |  2
C0014544  |  epilepsy  |  2
C0205770  |  choroid plexus papilloma  |  1
C0006118  |  brain tumors  |  1
C0020635  |  hypopituitarism  |  1
C0085666  |  capillary hemangioma  |  1
C0008780  |  ciliary dyskinesia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:4)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs369384363NA440193CCDC88Cumls:C0020255CLINVARNA0.12NACCDC88C1491338121GA,C
rs38790659721340693652BMP4umls:C0020255BeFreeA patient with anophthalmia, microphthalmia with sclerocornea, right-sided diaphragmatic hernia, and hydrocephalus was found to have a c.592C >T (p.R198X) nonsense mutation in BMP4.0.0002714422011BMP41453950667GC,A
rs387907320NA440193CCDC88Cumls:C0020255CLINVARNA0.12NACCDC88C1491277921CT
rs387907321NA440193CCDC88Cumls:C0020255CLINVARNA0.12NACCDC88C1491272870CT-
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:11)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0020255aminocaproic acidD01511960-32-2hydrocephalusMESH:D006849marker/mechanism20881558
C0020255caffeineD0021101958/8/2hydrocephalusMESH:D006849marker/mechanism5041373
C0020255carmustineD002330154-93-8hydrocephalusMESH:D006849marker/mechanism17334672
C0020255chloramphenicolD00270156-75-7hydrocephalusMESH:D006849marker/mechanism2041948
C0020255folic acidD00549259-30-3hydrocephalusMESH:D006849marker/mechanism14324085
C0020255linezolidD000069349-hydrocephalusMESH:D006849therapeutic18622679
C0020255methadoneD00869176-99-3hydrocephalusMESH:D006849marker/mechanism16997682
C0020255oxycodoneD01009876-42-6hydrocephalusMESH:D006849marker/mechanism20440598
C0020255tretinoinD014212302-79-4hydrocephalusMESH:D006849marker/mechanism1438063
C0020255valproic acidD01463599-66-1hydrocephalusMESH:D006849marker/mechanism12237071
C0020255vitamin aD01480111103-57-4hydrocephalusMESH:D006849marker/mechanism13410607
FDA approved drug and dosage information(Total Drugs:6)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D006849zyvoxlinezolid400MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsTABLET;ORALDiscontinuedNoneYesNo
MESH:D006849zyvoxlinezolid200MG/100ML (2MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesNo
MESH:D006849zyvoxlinezolid100MG/5MLFOR SUSPENSION;ORALPrescriptionABYesYes
MESH:D006849zyvoxlinezolid400MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsTABLET;ORALDiscontinuedNoneYesNo
MESH:D006849zyvoxlinezolid200MG/100ML (2MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesNo
MESH:D006849zyvoxlinezolid100MG/5MLFOR SUSPENSION;ORALPrescriptionABYesYes
FDA labeling changes(Total Drugs:6)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D00684912/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00684912/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00684912/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00684912/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'
MESH:D00684912/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'
MESH:D00684912/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'