pontocerebellar hypoplasia type 1
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Summary
pontocerebellar hypoplasia type 1 is a class of disease[1].
Key Facts
- pontocerebellar hypoplasia type 1's instance of is recorded as class of disease[2].
- pontocerebellar hypoplasia type 1's subclass of is recorded as non-syndromic pontocerebellar hypoplasia[3].
- pontocerebellar hypoplasia type 1's MeSH descriptor ID is recorded as C548069[4].
- pontocerebellar hypoplasia type 1's Orphanet ID is recorded as 2254[5].
- pontocerebellar hypoplasia type 1's genetic association is recorded as VRK1[6].
- pontocerebellar hypoplasia type 1's genetic association is recorded as EXOSC3[7].
- pontocerebellar hypoplasia type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2254[8].
- pontocerebellar hypoplasia type 1's UMLS CUI is recorded as C1843504[9].
- pontocerebellar hypoplasia type 1's UMLS CUI is recorded as C5442006[10].
- pontocerebellar hypoplasia type 1's ICD-10-CM is recorded as Q04.3[11].
- pontocerebellar hypoplasia type 1's GARD rare disease ID is recorded as 10704[12].
- pontocerebellar hypoplasia type 1's Mondo ID is recorded as MONDO_0016396[13].