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Multiple endocrine neoplasia type 2A
1 OMIM reference -
1 associated gene
23 connected diseases
No signs/symptoms info
Disease Type of connection
Hirschsprung disease
Bilateral renal agenesis
Bilateral renal dysplasia
Familial medullary thyroid carcinoma
Haddad syndrome
Multiple endocrine neoplasia type 2B
Papillary or follicular thyroid carcinoma
Unilateral renal dysplasia
Juvenile myelomonocytic leukemia
Noonan syndrome
Autosomal dominant hyper-IgE syndrome
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Hereditary gingival fibromatosis
Autosomal agammaglobulinemia
SHORT syndrome
Distal 22q11.2 microdeletion syndrome
LEOPARD syndrome
Metachondromatosis
Ondine syndrome
Synonym(s):
- MEN2A
- PTC syndrome
- Sipple syndrome
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: D018813
Gene symbol UniProt reference OMIM reference
RET P07949164761
No signs/symptoms info available.