pontocerebellar hypoplasia type 1A
human disease
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Summary
pontocerebellar hypoplasia type 1A is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- pontocerebellar hypoplasia type 1A's instance of is recorded as rare disease[3].
- pontocerebellar hypoplasia type 1A's instance of is recorded as class of disease[4].
- pontocerebellar hypoplasia type 1A is a type of non-syndromic pontocerebellar hypoplasia[5].
- pontocerebellar hypoplasia type 1A is a type of pontocerebellar hypoplasia type 1[6].
- pontocerebellar hypoplasia type 1A is a type of autosomal recessive disease[7].
- pontocerebellar hypoplasia type 1A's genetic association is recorded as VRK1[8].
- pontocerebellar hypoplasia type 1A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060265[9].
- pontocerebellar hypoplasia type 1A's exact match is recorded as http://identifiers.org/doid/DOID:0060265[10].
- pontocerebellar hypoplasia type 1A's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2254[11].
- pontocerebellar hypoplasia type 1A's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
pontocerebellar hypoplasia type 1A is known by 7 alternative names across languages and contexts.[2]