ODCs

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4 OMIM references -
4 associated genes
No signs/symptoms info

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Pontocerebellar hypoplasia type 2

Progressive cerebello-cerebral atrophy

Citations in the biomedical literature:

Pontocerebellar hypoplasia type 2		Progressive cerebello-cerebral atrophy
	Synonym(s): - PCH2		Synonym(s): - PCCA

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

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

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 4 OMIM references - 1 MeSH reference: C548070		External references: No OMIM references No MeSH references

No signs/symptoms info available.