MCID: TYP022
MIFTS: 5

Typical Urticaria Pigmentosa

Categories: Blood diseases, Rare diseases, Skin diseases

Aliases & Classifications for Typical Urticaria Pigmentosa

MalaCards integrated aliases for Typical Urticaria Pigmentosa:

Name: Typical Urticaria Pigmentosa 58

Classifications:

Orphanet: 58  
Rare skin diseases
Rare haematological diseases


External Ids:

ICD10 via Orphanet 33 Q82.2
Orphanet 58 ORPHA158766

Summaries for Typical Urticaria Pigmentosa

MalaCards based summary : Typical Urticaria Pigmentosa An important gene associated with Typical Urticaria Pigmentosa is KIT (KIT Proto-Oncogene, Receptor Tyrosine Kinase). Affiliated tissues include skin.

Related Diseases for Typical Urticaria Pigmentosa

Symptoms & Phenotypes for Typical Urticaria Pigmentosa

Drugs & Therapeutics for Typical Urticaria Pigmentosa

Search Clinical Trials , NIH Clinical Center for Typical Urticaria Pigmentosa

Genetic Tests for Typical Urticaria Pigmentosa

Anatomical Context for Typical Urticaria Pigmentosa

MalaCards organs/tissues related to Typical Urticaria Pigmentosa:

40
Skin

Publications for Typical Urticaria Pigmentosa

Variations for Typical Urticaria Pigmentosa

Expression for Typical Urticaria Pigmentosa

Search GEO for disease gene expression data for Typical Urticaria Pigmentosa.

Pathways for Typical Urticaria Pigmentosa

GO Terms for Typical Urticaria Pigmentosa

Sources for Typical Urticaria Pigmentosa

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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