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1 OMIM reference -
1 associated gene
1 sign/symptom
PROTEIN INTERACTIONS: 1
2 OMIM references -
1 associated gene
2 signs/symptoms
Pancreatic hypoplasia - diabetes - congenital heart disease
Benign familial chorea

GATA6 NKX2-1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GATA6
(0.72)
NKX2-1



Citations in the biomedical literature:


Pancreatic hypoplasia - diabetes - congenital heart disease
GATA6
Benign familial chorea
NKX2-1



Pancreatic hypoplasia - diabetes - congenital heart disease
Benign familial chorea

Synonym(s):
- Yorifuji-Okuno syndrome

Synonym(s):
- Hereditary benign chorea

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references

Pancreatic hypoplasia - diabetes - congenital heart disease
Benign familial chorea

Very frequent
- Stillbirth / neonatal death



Very frequent
- Abnormal gait
- Movement disorder