pontocerebellar hypoplasia type 2B
human disease
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pontocerebellar hypoplasia type 2B
Summary
pontocerebellar hypoplasia type 2B is a rare disease[1].
Key Facts
- pontocerebellar hypoplasia type 2B's instance of is recorded as rare disease[2].
- pontocerebellar hypoplasia type 2B's instance of is recorded as class of disease[3].
- pontocerebellar hypoplasia type 2B's subclass of is recorded as non-syndromic pontocerebellar hypoplasia[4].
- pontocerebellar hypoplasia type 2B's subclass of is recorded as pontocerebellar hypoplasia type 2[5].
- pontocerebellar hypoplasia type 2B's MeSH descriptor ID is recorded as C567325[6].
- pontocerebellar hypoplasia type 2B's OMIM ID is recorded as 612389[7].
- pontocerebellar hypoplasia type 2B's Disease Ontology ID is recorded as DOID:0060268[8].
- pontocerebellar hypoplasia type 2B's Orphanet ID is recorded as 2524[9].
- pontocerebellar hypoplasia type 2B's genetic association is recorded as TSEN2[10].
- pontocerebellar hypoplasia type 2B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060268[11].
- pontocerebellar hypoplasia type 2B's exact match is recorded as http://identifiers.org/doid/DOID:0060268[12].
- pontocerebellar hypoplasia type 2B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2524[13].
- pontocerebellar hypoplasia type 2B's UMLS CUI is recorded as C2676466[14].
- pontocerebellar hypoplasia type 2B's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- pontocerebellar hypoplasia type 2B's Mondo ID is recorded as MONDO_0012890[16].
- pontocerebellar hypoplasia type 2B's UniProt disease ID is recorded as DI-02177[17].