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1 OMIM reference -
1 associated gene
1 sign/symptom
COMMON GENES: 1
4 OMIM references -
3 associated genes
1 sign/symptom
Pancreatic hypoplasia - diabetes - congenital heart disease
Congenital diaphragmatic hernia

GATA6 FREM1
GATA6
ZFPM2


COMMON
GENES
GATA6



Citations in the biomedical literature:


Pancreatic hypoplasia - diabetes - congenital heart disease
GATA6
Congenital diaphragmatic hernia
FREM1 ZFPM2



Pancreatic hypoplasia - diabetes - congenital heart disease
Congenital diaphragmatic hernia

Synonym(s):
- Yorifuji-Okuno syndrome

Synonym(s):
- CDH
- Diaphragmatic agenesia

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare respiratory disease
- Rare surgical thoracic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: multigenic/multifactorial

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
1 MeSH reference: C538080

Pancreatic hypoplasia - diabetes - congenital heart disease
Congenital diaphragmatic hernia

Very frequent
- Stillbirth / neonatal death



Very frequent
- Diaphragmatic hernia / defect / agenesis