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Pediatric Disease Annotations & Medicines



   histiocytosis
  

Disease ID 915
Disease histiocytosis
Definition
General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT.
Synonym
histiocytic infiltrate
histiocytic infiltrate (morphologic abnormality)
histiocytic infiltrate, nos
histiocytic reaction
histiocytic reaction, nos
histiocytic syndrome
histiocytoses
histiocytosis (morphologic abnormality)
histiocytosis [disease/finding]
histiocytosis, nos
histiocytosis, unspecified
histiocytosis, unspecified (disorder)
reticuloendothelial cell infiltrate
reticuloendothelial cell infiltrate, nos
reticulohistiocytosis
reticulohistiocytosis, nos
DOID
UMLS
C0019618
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:59)
C0011847  |  diabetes  |  5
C0024299  |  lymphoma  |  5
C0011848  |  diabetes insipidus  |  4
C0003873  |  rheumatoid arthritis  |  3
C0079748  |  lymphoblastic lymphoma  |  2
C0032285  |  pneumonia  |  2
C0242647  |  mucosa-associated lymphoid tissue  |  2
C0598894  |  monocytic leukemia  |  2
C0687720  |  central diabetes insipidus  |  2
C0007115  |  thyroid ca  |  2
C0549473  |  thyroid carcinoma  |  2
C0020542  |  pulmonary hypertension  |  2
C0238463  |  papillary thyroid carcinoma  |  2
C0684249  |  carcinoma of the lung  |  1
C0008370  |  cholestasis  |  1
C0023467  |  acute myeloid leukemia  |  1
C0015624  |  fanconi syndrome  |  1
C0019829  |  hodgkin's lymphoma  |  1
C0007134  |  renal cell carcinoma  |  1
C0152013  |  adenocarcinoma of the lung  |  1
C0175703  |  tar syndrome  |  1
C0024214  |  lymphangiectasia  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0242647  |  marginal zone b-cell lymphoma  |  1
C0023895  |  liver disease  |  1
C0023470  |  myeloid leukemia  |  1
C0242647  |  mucosa-associated lymphoid tissue lymphoma  |  1
C0011854  |  insulin dependent diabetes mellitus  |  1
C0011854  |  insulin dependent diabetes  |  1
C0029408  |  osteoarthritis  |  1
C0079731  |  b-cell lymphoma  |  1
C0085669  |  acute leukemia  |  1
C0020305  |  hydrops fetalis  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0032226  |  pleural disease  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0011615  |  atopic dermatitis  |  1
C0023467  |  acute myeloid leukaemia  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0020538  |  hypertension  |  1
C0948303  |  peritoneal carcinoma  |  1
C0002726  |  amyloidosis  |  1
C0032131  |  plasmacytoma  |  1
C0007137  |  squamous cell carcinoma  |  1
C0078981  |  arachnoid cyst  |  1
C0032326  |  pneumothorax  |  1
C0024115  |  lung disorders  |  1
C0085669  |  acute leukemias  |  1
C0021933  |  intussusception  |  1
C1136085  |  monoclonal gammopathy  |  1
C0029443  |  osteomyelitis  |  1
C0023470  |  myeloid leukaemia  |  1
C0878675  |  erdheim-chester disease  |  1
C1261473  |  sarcoma  |  1
C0029182  |  orbital disease  |  1
C0004030  |  aspergillosis  |  1
C1527336  |  sjogren's syndrome  |  1
C0001418  |  adenocarcinoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
NPC2  |  10577  |  UniProtKB-KW;GHR
SMPD1  |  6609  |  UniProtKB-KW;GHR
NPC1  |  4864  |  UniProtKB-KW;GHR
BRAF  |  673  |  GHR
SLC29A3  |  55315  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:223)
4074  |  M6PR  |  DISEASES
6362  |  CCL18  |  DISEASES
3385  |  ICAM3  |  DISEASES
4680  |  CEACAM6  |  DISEASES
201294  |  UNC13D  |  DISEASES
50487  |  PLA2G3  |  DISEASES
410  |  ARSA  |  DISEASES
54  |  ACP5  |  DISEASES
23659  |  PLA2G15  |  DISEASES
10404  |  CPQ  |  DISEASES
6813  |  STXBP2  |  DISEASES
973  |  CD79A  |  DISEASES
7431  |  VIM  |  DISEASES
952  |  CD38  |  DISEASES
3558  |  IL2  |  DISEASES
9733  |  SART3  |  DISEASES
3458  |  IFNG  |  DISEASES
2026  |  ENO2  |  DISEASES
5564  |  PRKAB1  |  DISEASES
7942  |  TFEB  |  DISEASES
3565  |  IL4  |  DISEASES
1509  |  CTSD  |  DISEASES
335  |  APOA1  |  DISEASES
9525  |  VPS4B  |  DISEASES
8600  |  TNFSF11  |  DISEASES
718  |  C3  |  DISEASES
1236  |  CCR7  |  DISEASES
968  |  CD68  |  DISEASES
348  |  APOE  |  DISEASES
2670  |  GFAP  |  DISEASES
5565  |  PRKAB2  |  DISEASES
6382  |  SDC1  |  DISEASES
27183  |  VPS4A  |  DISEASES
1401  |  CRP  |  DISEASES
23640  |  HSPBP1  |  DISEASES
9398  |  CD101  |  DISEASES
5156  |  PDGFRA  |  DISEASES
90070  |  LACRT  |  DISEASES
6610  |  SMPD2  |  DISEASES
3569  |  IL6  |  DISEASES
3557  |  IL1RN  |  DISEASES
3685  |  ITGAV  |  DISEASES
4069  |  LYZ  |  DISEASES
999  |  CDH1  |  DISEASES
6505  |  SLC1A1  |  DISEASES
5862  |  RAB2A  |  DISEASES
5264  |  PHYH  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
79968  |  WDR76  |  DISEASES
5007  |  OSBP  |  DISEASES
943  |  TNFRSF8  |  DISEASES
5290  |  PIK3CA  |  DISEASES
3931  |  LCAT  |  DISEASES
60482  |  SLC5A7  |  DISEASES
941  |  CD80  |  DISEASES
5443  |  POMC  |  DISEASES
3383  |  ICAM1  |  DISEASES
950  |  SCARB2  |  DISEASES
7879  |  RAB7A  |  DISEASES
29999  |  FSCN3  |  DISEASES
3189  |  HNRNPH3  |  DISEASES
51411  |  BIN2  |  DISEASES
3073  |  HEXA  |  DISEASES
3687  |  ITGAX  |  DISEASES
4864  |  NPC1  |  DISEASES
7157  |  TP53  |  DISEASES
63976  |  PRDM16  |  DISEASES
285362  |  SUMF1  |  DISEASES
6769  |  STAC  |  DISEASES
85417  |  CCNB3  |  DISEASES
23196  |  FAM120A  |  DISEASES
7070  |  THY1  |  DISEASES
7345  |  UCHL1  |  DISEASES
23643  |  LY96  |  DISEASES
5018  |  OXA1L  |  DISEASES
1436  |  CSF1R  |  DISEASES
3156  |  HMGCR  |  DISEASES
3815  |  KIT  |  DISEASES
673  |  BRAF  |  DISEASES
909  |  CD1A  |  DISEASES
29881  |  NPC1L1  |  DISEASES
50848  |  F11R  |  DISEASES
6285  |  S100B  |  DISEASES
6271  |  S100A1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
134429  |  STARD4  |  DISEASES
3562  |  IL3  |  DISEASES
1437  |  CSF2  |  DISEASES
84889  |  SLC7A3  |  DISEASES
5267  |  SERPINA4  |  DISEASES
290  |  ANPEP  |  DISEASES
5604  |  MAP2K1  |  DISEASES
340024  |  SLC6A19  |  DISEASES
84342  |  COG8  |  DISEASES
2548  |  GAA  |  DISEASES
2720  |  GLB1  |  DISEASES
153572  |  IRX2  |  DISEASES
9451  |  EIF2AK3  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
7368  |  UGT8  |  DISEASES
924  |  CD7  |  DISEASES
23166  |  STAB1  |  DISEASES
2629  |  GBA  |  DISEASES
30835  |  CD209  |  DISEASES
4684  |  NCAM1  |  DISEASES
3321  |  IGSF3  |  DISEASES
4018  |  LPA  |  DISEASES
3039  |  HBA1  |  DISEASES
1435  |  CSF1  |  DISEASES
284359  |  IZUMO1  |  DISEASES
3563  |  IL3RA  |  DISEASES
5155  |  PDGFB  |  DISEASES
942  |  CD86  |  DISEASES
10227  |  MFSD10  |  DISEASES
256933  |  NPB  |  DISEASES
3916  |  LAMP1  |  DISEASES
3988  |  LIPA  |  DISEASES
23583  |  SMUG1  |  DISEASES
857  |  CAV1  |  DISEASES
3805  |  KIR2DL4  |  DISEASES
4602  |  MYB  |  DISEASES
6609  |  SMPD1  |  DISEASES
5781  |  PTPN11  |  DISEASES
2583  |  B4GALNT1  |  DISEASES
1508  |  CTSB  |  DISEASES
921  |  CD5  |  DISEASES
57515  |  SERINC1  |  DISEASES
9514  |  GAL3ST1  |  DISEASES
3605  |  IL17A  |  DISEASES
53827  |  FXYD5  |  DISEASES
26762  |  HAVCR1  |  DISEASES
347  |  APOD  |  DISEASES
57556  |  SEMA6A  |  DISEASES
355  |  FAS  |  DISEASES
26503  |  SLC17A5  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3683  |  ITGAL  |  DISEASES
2760  |  GM2A  |  DISEASES
1510  |  CTSE  |  DISEASES
4763  |  NF1  |  DISEASES
404552  |  SCGB1D4  |  DISEASES
2526  |  FUT4  |  DISEASES
6364  |  CCL20  |  DISEASES
51454  |  GULP1  |  DISEASES
9332  |  CD163  |  DISEASES
6832  |  SUPV3L1  |  DISEASES
93034  |  NT5C1B  |  DISEASES
7037  |  TFRC  |  DISEASES
6693  |  SPN  |  DISEASES
4311  |  MME  |  DISEASES
10210  |  TOPORS  |  DISEASES
6721  |  SREBF2  |  DISEASES
1378  |  CR1  |  DISEASES
1380  |  CR2  |  DISEASES
1118  |  CHIT1  |  DISEASES
5788  |  PTPRC  |  DISEASES
5321  |  PLA2G4A  |  DISEASES
8676  |  STX11  |  DISEASES
2214  |  FCGR3A  |  DISEASES
910  |  CD1B  |  DISEASES
911  |  CD1C  |  DISEASES
10924  |  SMPDL3A  |  DISEASES
6280  |  S100A9  |  DISEASES
4942  |  OAT  |  DISEASES
1520  |  CTSS  |  DISEASES
914  |  CD2  |  DISEASES
965  |  CD58  |  DISEASES
4893  |  NRAS  |  DISEASES
5309  |  PITX3  |  DISEASES
89885  |  FATE1  |  DISEASES
959  |  CD40LG  |  DISEASES
5236  |  PGM1  |  DISEASES
4068  |  SH2D1A  |  DISEASES
56623  |  INPP5E  |  DISEASES
27069  |  GHITM  |  DISEASES
5476  |  CTSA  |  DISEASES
55315  |  SLC29A3  |  DISEASES
2934  |  GSN  |  DISEASES
2268  |  FGR  |  DISEASES
7357  |  UGCG  |  DISEASES
367  |  AR  |  DISEASES
19  |  ABCA1  |  DISEASES
50943  |  FOXP3  |  DISEASES
369  |  ARAF  |  DISEASES
54880  |  BCOR  |  DISEASES
9308  |  CD83  |  DISEASES
3559  |  IL2RA  |  DISEASES
2665  |  GDI2  |  DISEASES
551  |  AVP  |  DISEASES
414  |  ARSD  |  DISEASES
427  |  ASAH1  |  DISEASES
6624  |  FSCN1  |  DISEASES
10522  |  DEAF1  |  DISEASES
238  |  ALK  |  DISEASES
3681  |  ITGAD  |  DISEASES
12  |  SERPINA3  |  DISEASES
5660  |  PSAP  |  DISEASES
6696  |  SPP1  |  DISEASES
5609  |  MAP2K7  |  DISEASES
50489  |  CD207  |  DISEASES
9842  |  PLEKHM1  |  DISEASES
197  |  AHSG  |  DISEASES
5538  |  PPT1  |  DISEASES
7124  |  TNF  |  DISEASES
7072  |  TIA1  |  DISEASES
5229  |  PGGT1B  |  DISEASES
7812  |  CSDE1  |  DISEASES
3586  |  IL10  |  DISEASES
57670  |  KIAA1549  |  DISEASES
338376  |  IFNE  |  DISEASES
9367  |  RAB9A  |  DISEASES
84000  |  TMPRSS13  |  DISEASES
727897  |  MUC5B  |  DISEASES
441864  |  TARM1  |  DISEASES
3684  |  ITGAM  |  DISEASES
10577  |  NPC2  |  DISEASES
100288687  |  DUX4  |  DISEASES
653545  |  DUX4L5  |  DISEASES
348120  |  LINC01193  |  DISEASES
79104  |  MEG8  |  DISEASES
4555  |  MT-TD  |  DISEASES
Locus(Waiting for update.)
Disease ID 915
Disease histiocytosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:44)
HP:0002716  |  Lymph node hyperplasia  |  110
HP:0002665  |  Lymphoma  |  5
HP:0000873  |  Diabetes insipidus  |  4
HP:0001370  |  Rheumatoid arthritis  |  3
HP:0002664  |  Neoplasia  |  3
HP:0002895  |  Papillary thyroid carcinoma  |  2
HP:0002890  |  Thyroid carcinoma  |  2
HP:0000863  |  Neurohypophyseal diabetes insipidus  |  2
HP:0002092  |  Pulmonary artery hypertension  |  2
HP:0002090  |  Pneumonia  |  2
HP:0012325  |  Chronic myelomonocytic leukemia  |  2
HP:0001789  |  Hydrops fetalis  |  1
HP:0100242  |  Sarcoma  |  1
HP:0001047  |  Atopic dermatitis  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0002576  |  Intussusception  |  1
HP:0000969  |  Dropsy  |  1
HP:0002593  |  Intestinal lymphangiectasia  |  1
HP:0001396  |  Cholestasis  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0002835  |  Aspiration  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0002318  |  Cervical myelopathy  |  1
HP:0040189  |  Desquamation  |  1
HP:0100702  |  Arachnoid cyst  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0001397  |  Hepatic steatosis  |  1
HP:0000078  |  Genital abnormalities  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0030731  |  Carcinoma  |  1
HP:0002758  |  Osteoarthritis  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0011857  |  Plasmacytoma  |  1
HP:0002107  |  Collapsed lung  |  1
HP:0002754  |  Bone infection  |  1
HP:0002488  |  Acute leukemias  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0001994  |  'de toni-fanconi-debre' syndrome  |  1
HP:0100825  |  Inflammation of the lips  |  1
HP:0000822  |  Hypertension  |  1
Disease ID 915
Disease histiocytosis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:3)
C2363896  |  hypothalamic diabetes insipidus
C2186532  |  liver disease
C0376293  |  stigmata
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0023895  |  liver disease  |  1
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.)