ODCs

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

PROTEIN INTERACTIONS: 1

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

Rhizomelic chondrodysplasia punctata type 2

Rhizomelic chondrodysplasia punctata type 3


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GNPAT	(0.79)	AGPS

Citations in the biomedical literature:

Rhizomelic chondrodysplasia punctata type 2		Rhizomelic chondrodysplasia punctata type 3

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease

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

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

No signs/symptoms info available.