pontocerebellar hypoplasia type 3

Summary

pontocerebellar hypoplasia type 3 is a developmental defect during embryogenesis^[1].

Key Facts

• pontocerebellar hypoplasia type 3's instance of is recorded as developmental defect during embryogenesis^[2].
• pontocerebellar hypoplasia type 3's instance of is recorded as rare disease^[3].
• pontocerebellar hypoplasia type 3's instance of is recorded as class of disease^[4].
• pontocerebellar hypoplasia type 3's subclass of is recorded as non-syndromic pontocerebellar hypoplasia^[5].
• pontocerebellar hypoplasia type 3's MeSH descriptor ID is recorded as C548072^[6].
• pontocerebellar hypoplasia type 3's OMIM ID is recorded as 608027^[7].
• pontocerebellar hypoplasia type 3's Disease Ontology ID is recorded as DOID:0060272^[8].
• pontocerebellar hypoplasia type 3's Orphanet ID is recorded as 97249^[9].
• pontocerebellar hypoplasia type 3's genetic association is recorded as PCLO^[10].
• pontocerebellar hypoplasia type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060272^[11].
• pontocerebellar hypoplasia type 3's exact match is recorded as http://identifiers.org/doid/DOID:0060272^[12].
• pontocerebellar hypoplasia type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97249^[13].
• pontocerebellar hypoplasia type 3's UMLS CUI is recorded as C1842687^[14].
• pontocerebellar hypoplasia type 3's ICD-10-CM is recorded as Q04.3^[15].
• pontocerebellar hypoplasia type 3's GARD rare disease ID is recorded as 10708^[16].
• pontocerebellar hypoplasia type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• pontocerebellar hypoplasia type 3's Mondo ID is recorded as MONDO_0011948^[18].
• pontocerebellar hypoplasia type 3's UniProt disease ID is recorded as DI-04470^[19].