ODCs

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2 OMIM references -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Microtia

Microlissencephaly


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HOXA2	(0.63)	NDE1

Citations in the biomedical literature:

Microtia		Microlissencephaly

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare otorhinolaryngologic disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - 1 MeSH reference: C537772		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.