pontocerebellar hypoplasia type 2
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pontocerebellar hypoplasia type 2
Summary
pontocerebellar hypoplasia type 2 is a class of disease[1].
Key Facts
- pontocerebellar hypoplasia type 2's instance of is recorded as class of disease[2].
- pontocerebellar hypoplasia type 2's subclass of is recorded as non-syndromic pontocerebellar hypoplasia[3].
- pontocerebellar hypoplasia type 2's MeSH descriptor ID is recorded as C548070[4].
- pontocerebellar hypoplasia type 2's Orphanet ID is recorded as 2524[5].
- pontocerebellar hypoplasia type 2's NCI Thesaurus ID is recorded as C124057[6].
- pontocerebellar hypoplasia type 2's genetic association is recorded as SEPSECS[7].
- pontocerebellar hypoplasia type 2's genetic association is recorded as TSEN2[8].
- pontocerebellar hypoplasia type 2's genetic association is recorded as TSEN54[9].
- pontocerebellar hypoplasia type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2524[10].
- pontocerebellar hypoplasia type 2's UMLS CUI is recorded as C2932714[11].
- pontocerebellar hypoplasia type 2's ICD-10-CM is recorded as Q04.3[12].
- pontocerebellar hypoplasia type 2's GARD rare disease ID is recorded as 10705[13].
- pontocerebellar hypoplasia type 2's Mondo ID is recorded as MONDO_0016759[14].