Disease #04088 (PCH-10 (hypoplasia, pontocerebellar, type 10 (PCH-10)), OMIM:615803)

Official abbreviation PCH-10
Name hypoplasia, pontocerebellar, type 10 (PCH-10)
OMIM ID 615803
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CLP1
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Disease features -
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Individuals

1 entry on 1 page. Showing entry 1.
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00080985 - PubMed: Trujillano 2017 unaffected parents - - - - - 0 - - PCH-10 Pontocerebellar hypoplasia, type 10 (OMIM:615803) CLP1 CLP1 1 1 Daniel Trujillano
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