Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   obstructive hydrocephalus
  

Disease ID 1760
Disease obstructive hydrocephalus
Definition
An abnormal accumulation of cerebrospinal fluid within the ventricles of the brain that occurs as a consequence of an obstruction at any location within the ventricular system that prevents cerebrospinal fluid flowing into the subarachnoid space.
Synonym
hydrocephalus, noncommunicating
hydrocephalus, obstructive
non-communicating hydrocephalus
obstructiv hydrocephalus
obstructive hydrocephalus (disorder)
DOID
ICD10
UMLS
C0549423
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:31)
C0151740  |  increased intracranial pressure  |  5
C0151740  |  intracranial hypertension  |  4
C0025289  |  meningitis  |  3
C0020538  |  hypertension  |  2
C0025309  |  meningoencephalitis  |  1
C0152013  |  lung adenocarcinoma  |  1
C0010276  |  craniopharyngiomas  |  1
C0010276  |  craniopharyngioma  |  1
C0040558  |  toxoplasmosis  |  1
C0151740  |  elevated intracranial pressure  |  1
C0334583  |  pilocytic astrocytoma  |  1
C0879615  |  stromal tumor  |  1
C0041318  |  tuberculous meningitis  |  1
C0917996  |  cerebral aneurysm  |  1
C0078981  |  arachnoid cyst  |  1
C0001418  |  adenocarcinoma  |  1
C0032285  |  pneumoniae  |  1
C0040053  |  thrombosis  |  1
C0085273  |  parvovirus b19 infection  |  1
C0012569  |  diplopia  |  1
C0238198  |  gastrointestinal stromal tumor  |  1
C0037198  |  sinus thrombosis  |  1
C0026934  |  mycoplasma  |  1
C1332900  |  cerebellar hemangioblastoma  |  1
C0004114  |  astrocytoma  |  1
C0020255  |  hydrocephalus  |  1
C0085315  |  cns toxoplasmosis  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0206660  |  germinoma  |  1
C0206734  |  hemangioblastoma  |  1
C0151740  |  raised intracranial pressure  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:81)
10301  |  DLEU1  |  DISEASES
2288  |  FKBP4  |  DISEASES
7249  |  TSC2  |  DISEASES
5327  |  PLAT  |  DISEASES
2026  |  ENO2  |  DISEASES
4488  |  MSX2  |  DISEASES
10804  |  GJB6  |  DISEASES
2670  |  GFAP  |  DISEASES
6538  |  SLC6A11  |  DISEASES
3021  |  H3F3B  |  DISEASES
4440  |  MSI1  |  DISEASES
10241  |  CALCOCO2  |  DISEASES
23314  |  SATB2  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
4591  |  TRIM37  |  DISEASES
9368  |  SLC9A3R1  |  DISEASES
6855  |  SYP  |  DISEASES
90  |  ACVR1  |  DISEASES
10000  |  AKT3  |  DISEASES
390  |  RND3  |  DISEASES
2121  |  EVC  |  DISEASES
7157  |  TP53  |  DISEASES
285362  |  SUMF1  |  DISEASES
5921  |  RASA1  |  DISEASES
4715  |  NDUFB9  |  DISEASES
23657  |  SLC7A11  |  DISEASES
7082  |  TJP1  |  DISEASES
2895  |  GRID2  |  DISEASES
4838  |  NODAL  |  DISEASES
7547  |  ZIC3  |  DISEASES
2177  |  FANCD2  |  DISEASES
2176  |  FANCC  |  DISEASES
1278  |  COL1A2  |  DISEASES
5617  |  PRL  |  DISEASES
5340  |  PLG  |  DISEASES
358  |  AQP1  |  DISEASES
8557  |  TCAP  |  DISEASES
2302  |  FOXJ1  |  DISEASES
1641  |  DCX  |  DISEASES
5873  |  RAB27A  |  DISEASES
6540  |  SLC6A13  |  DISEASES
113675  |  SDSL  |  DISEASES
4771  |  NF2  |  DISEASES
4763  |  NF1  |  DISEASES
4478  |  MSN  |  DISEASES
2475  |  MTOR  |  DISEASES
3020  |  H3F3A  |  DISEASES
3664  |  IRF6  |  DISEASES
8676  |  STX11  |  DISEASES
7062  |  TCHH  |  DISEASES
4803  |  NGF  |  DISEASES
51684  |  SUFU  |  DISEASES
6005  |  RHAG  |  DISEASES
5728  |  PTEN  |  DISEASES
1025  |  CDK9  |  DISEASES
5081  |  PAX7  |  DISEASES
1325  |  CORT  |  DISEASES
317762  |  CCDC85C  |  DISEASES
427  |  ASAH1  |  DISEASES
26278  |  SACS  |  DISEASES
4487  |  MSX1  |  DISEASES
361  |  AQP4  |  DISEASES
9901  |  SRGAP3  |  DISEASES
5077  |  PAX3  |  DISEASES
9244  |  CRLF1  |  DISEASES
5091  |  PC  |  DISEASES
174  |  AFP  |  DISEASES
3166  |  HMX1  |  DISEASES
501  |  ALDH7A1  |  DISEASES
9048  |  ARTN  |  DISEASES
1875  |  E2F5  |  DISEASES
6559  |  SLC12A3  |  DISEASES
139728  |  PNCK  |  DISEASES
284252  |  KCTD1  |  DISEASES
2668  |  GDNF  |  DISEASES
2263  |  FGFR2  |  DISEASES
4140  |  MARK3  |  DISEASES
627  |  BDNF  |  DISEASES
83695  |  RHNO1  |  DISEASES
6642  |  SNX1  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1760
Disease obstructive hydrocephalus
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:36)
HP:0002516  |  Intracranial pressure elevation  |  9
HP:0002664  |  Neoplasia  |  6
HP:0002315  |  Headaches  |  4
HP:0001287  |  Meningitis  |  3
HP:0002410  |  Aqueductal stenosis  |  3
HP:0011695  |  Cerebellar hemorrhage  |  2
HP:0002119  |  Ventricular dilatation  |  2
HP:0000822  |  Hypertension  |  2
HP:0000969  |  Dropsy  |  2
HP:0012683  |  Pineal cyst  |  2
HP:0100702  |  Arachnoid cyst  |  1
HP:0000651  |  Diplopia  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0004490  |  Hyperostosis of calvarial bones  |  1
HP:0002615  |  Low blood pressure  |  1
HP:0030062  |  Craniopharyngioma  |  1
HP:0010797  |  Hemangioblastoma  |  1
HP:0005305  |  Cerebral vein thrombosis  |  1
HP:0001270  |  Motor retardation  |  1
HP:0006880  |  Hemangioblastoma, sporadic cerebellar  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0002344  |  Progressive neurologic deterioration  |  1
HP:0009592  |  Astrocytoma  |  1
HP:0002018  |  Nausea  |  1
HP:0030078  |  Lung adenocarcinoma  |  1
HP:0001263  |  Developmental retardation  |  1
HP:0030746  |  Intraventricular hemorrhage  |  1
HP:0001289  |  Confusion  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0030692  |  Brain tumor  |  1
HP:0100723  |  Gastrointestinal stroma tumor  |  1
HP:0012062  |  Bone cysts  |  1
HP:0012063  |  Aneurysmal bone cyst  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0009733  |  Glioma  |  1
HP:0004944  |  Cerebral artery aneurysm  |  1
Disease ID 1760
Disease obstructive hydrocephalus
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)