MCID: HRD197
MIFTS: 6

Hereditary Pediatric Behçet-Like Disease malady

Categories: Bone diseases, Rare diseases

Aliases & Classifications for Hereditary Pediatric Behçet-Like Disease

Aliases & Descriptions for Hereditary Pediatric Behçet-Like Disease:

Name: Hereditary Pediatric Behçet-Like Disease 56
Behçet-Like Disease Due to Haploinsufficiency of A20 56
Behçet-Like Disease Due to Ha20 56

Classifications:



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Summaries for Hereditary Pediatric Behçet-Like Disease

MalaCards based summary : Hereditary Pediatric Behçet-Like Disease, is also known as behçet-like disease due to haploinsufficiency of a20. An important gene associated with Hereditary Pediatric Behçet-Like Disease is TNFAIP3 (TNF Alpha Induced Protein 3). Affiliated tissues include bone.

Related Diseases for Hereditary Pediatric Behçet-Like Disease

Symptoms & Phenotypes for Hereditary Pediatric Behçet-Like Disease

Drugs & Therapeutics for Hereditary Pediatric Behçet-Like Disease

Search Clinical Trials , NIH Clinical Center for Hereditary Pediatric Behçet-Like Disease

Genetic Tests for Hereditary Pediatric Behçet-Like Disease

Anatomical Context for Hereditary Pediatric Behçet-Like Disease

MalaCards organs/tissues related to Hereditary Pediatric Behçet-Like Disease:

39
Bone

Publications for Hereditary Pediatric Behçet-Like Disease

Variations for Hereditary Pediatric Behçet-Like Disease

Expression for Hereditary Pediatric Behçet-Like Disease

Search GEO for disease gene expression data for Hereditary Pediatric Behçet-Like Disease.

Pathways for Hereditary Pediatric Behçet-Like Disease

GO Terms for Hereditary Pediatric Behçet-Like Disease

Sources for Hereditary Pediatric Behçet-Like Disease

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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