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Combined pituitary hormone deficiencies, genetic forms
4 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
MITF-related melanoma and renal cell carcinoma predisposition syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Combined pituitary hormone deficiencies, genetic forms
MITF-related melanoma and renal cell carcinoma predisposition syndrome

GLI2
(UniProt - OMIM)
 MITF
(UniProt - OMIM)
HESX1
(UniProt - OMIM)
OTX2
(UniProt - OMIM)
POU1F1
(UniProt - OMIM)
PROP1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
OTX2
(0.52)
MITF


Citations in the biomedical literature:


Combined pituitary hormone deficiencies, genetic forms
GLI2 HESX1 OTX2 POU1F1 PROP1
MITF-related melanoma and renal cell carcinoma predisposition syndrome
MITF



Combined pituitary hormone deficiencies, genetic forms
MITF-related melanoma and renal cell carcinoma predisposition syndrome

Synonym(s):
- Familial congenital hypopituitarism
- Multiple pituitary hormone deficiencies, genetic forms
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare infertility
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.