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Estrogen resistance syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
2 OMIM references -
1 associated gene
No signs/symptoms info
Estrogen resistance syndrome
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency

ESR1
(UniProt - OMIM)
 HADH
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ESR1
(0.63)
HADH


Citations in the biomedical literature:


Estrogen resistance syndrome
ESR1
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
HADH



Estrogen resistance syndrome
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- HADH deficiency
- Hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Hyperinsulinism due to HADH deficiency
- Hyperinsulinism due to SCHAD deficiency
- Hyperinsulinism due to glutamodehydrogenase deficiency
- SCHAD deficiency
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.