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Familial papillary renal cell carcinoma
1 OMIM reference -
1 associated gene
55 connected diseases
No signs/symptoms info
Disease Type of connection
Hepatocellular carcinoma, childhood-onset
Juvenile myelomonocytic leukemia
Noonan syndrome
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Opsismodysplasia
LEOPARD syndrome
Metachondromatosis
Giant cell glioblastoma
Gliosarcoma
Autosomal agammaglobulinemia
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Pilomatrixoma
SHORT syndrome
Glomuvenous malformation
Autosomal dominant hyper-IgE syndrome
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Autosomal recessive lymphoproliferative disease
Capillary malformation - arteriovenous malformation
Cherubism
Combined immunodeficiency due to ZAP70 deficiency
Distal 16p11.2 microdeletion syndrome
Familial gastric cancer
Gastric linitis plastica
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Hereditary gingival fibromatosis
MODY syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
PLCG2-associated antibody deficiency and immune dysregulation
Parkes Weber syndrome
Proximal 16p11.2 microdeletion syndrome
Severe combined immunodeficiency due to LCK deficiency
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
X-linked lymphoproliferative disease
Congenital stromal corneal dystrophy
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
T-B+ severe combined immunodeficiency due to CD45 deficiency
Cerebellar ataxia - hypogonadism
Cornelia de Lange syndrome
Familial capillary hemangioma
Epidermolysis bullosa simplex with pyloric atresia
Generalized junctional epidermolysis bullosa, non-Herlitz type
Junctional epidermolysis bullosa - pyloric atresia
Localized junctional epidermolysis bullosa, non-Herlitz type
Autoimmune lymphoproliferative syndrome
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C538614
Gene symbol UniProt reference OMIM reference
MET P08581164860
No signs/symptoms info available.