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Glomuvenous malformation
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Familial papillary renal cell carcinoma
Hepatocellular carcinoma, childhood-onset
Pseudohypoaldosteronism type 2E
Synonym(s):
- Glomangiomatosis
- Hereditary multiple glomangiomas
- Multiple glomus tumors
- VMGLOM
- Venous malformations with glomus cells
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C536827
Gene symbol UniProt reference OMIM reference
GLMN Q92990601749
No signs/symptoms info available.