pontocerebellar hypoplasia type 10
human disease
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Summary
pontocerebellar hypoplasia type 10 is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- pontocerebellar hypoplasia type 10's instance of is recorded as developmental defect during embryogenesis[3].
- pontocerebellar hypoplasia type 10's instance of is recorded as rare disease[4].
- pontocerebellar hypoplasia type 10's instance of is recorded as class of disease[5].
- pontocerebellar hypoplasia type 10 is a type of non-syndromic pontocerebellar hypoplasia[6].
- pontocerebellar hypoplasia type 10's genetic association is recorded as CLP1[7].
- pontocerebellar hypoplasia type 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060279[8].
- pontocerebellar hypoplasia type 10's exact match is recorded as http://identifiers.org/doid/DOID:0060279[9].
- pontocerebellar hypoplasia type 10's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_411493[10].
- pontocerebellar hypoplasia type 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
pontocerebellar hypoplasia type 10 is known by 5 alternative names across languages and contexts.[2]