ODCs

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4 OMIM references -
3 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
7 signs/symptoms

Congenital diaphragmatic hernia

Beta-thalassemia - X-linked thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ZFPM2	(0.87)	GATA1

Citations in the biomedical literature:

Congenital diaphragmatic hernia		Beta-thalassemia - X-linked thrombocytopenia
	Synonym(s): - CDH - Diaphragmatic agenesia		Synonym(s): - XLTT

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive

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

Congenital diaphragmatic hernia		Beta-thalassemia - X-linked thrombocytopenia
	Very frequent - Diaphragmatic hernia / defect / agenesis		Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding - Platelets function anomaly - Splenomegaly - Thrombocytopenia / thrombopenia - X-linked recessive inheritance