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Congenital diaphragmatic hernia

4 OMIM references -
3 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Brain-lung-thyroid syndrome

1 OMIM reference -
1 associated gene
No signs/symptoms info

Congenital diaphragmatic hernia

Brain-lung-thyroid syndrome

FREM1	(UniProt - OMIM)		NKX2-1	(UniProt - OMIM)
GATA6	(UniProt - OMIM)
ZFPM2	(UniProt - OMIM)


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

Citations in the biomedical literature:

Congenital diaphragmatic hernia		Brain-lung-thyroid syndrome
	Synonym(s): - CDH - Diaphragmatic agenesia		Synonym(s): - Choreoathetosis - hypothyroidism - neonatal respiratory distress

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Certain conditions originating in the perinatal period -

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

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

Congenital diaphragmatic hernia
	Very frequent - Diaphragmatic hernia / defect / agenesis
Brain-lung-thyroid syndrome
(no data available)