ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Hypochondrogenesis

Fetal and neonatal alloimmune thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL2A1	(0.85)	ITGA2B

Citations in the biomedical literature:

Hypochondrogenesis		Fetal and neonatal alloimmune thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - NAIT

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare hematologic 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: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.