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Familial renal cell carcinoma
6 associated genes
18 connected diseases
No signs/symptoms info
Disease Type of connection
Papillary or follicular thyroid carcinoma
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Chuvash erythrocytosis
Von Hippel-Lindau disease
Autosomal recessive spastic paraplegia type 18
Dedifferentiated liposarcoma
Juvenile primary lateral sclerosis
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Well-differentiated liposarcoma
Familial amyloidosis, Finnish type
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: C536851
No signs/symptoms info available.