ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Chudley-McCullough syndrome

Phakomatosis pigmentokeratotica


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GPSM2	(0.73)	HRAS

Citations in the biomedical literature:

Chudley-McCullough syndrome		Phakomatosis pigmentokeratotica

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: C537893

No signs/symptoms info available.