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T-cell immunodeficiency with epidermodysplasia verruciformis
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial short QT syndrome
Romano-Ward syndrome
X-linked non-syndromic intellectual deficit
Familial thoracic aortic aneurysm and aortic dissection
Loeys-Dietz syndrome type 1
Multiple keratoacanthoma, Ferguson-Smith type
Synonym(s):
- T-cell immunodeficiency due to RHOH deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
RHOH Q15669602037
No signs/symptoms info available.