omodysplasia

Summary

omodysplasia is a rare disease^[1].

Key Facts

• omodysplasia's instance of is recorded as rare disease^[2].
• omodysplasia's instance of is recorded as class of disease^[3].
• omodysplasia's subclass of is recorded as osteochondrodysplasia^[4].
• omodysplasia's MeSH descriptor ID is recorded as C567664^[5].
• omodysplasia's MeSH descriptor ID is recorded as C537746^[6].
• omodysplasia's OMIM ID is recorded as 258315^[7].
• omodysplasia's OMIM ID is recorded as 164745^[8].
• omodysplasia's ICD-10 ID is recorded as Q78.8^[9].
• omodysplasia's KEGG ID is recorded as H02154^[10].
• omodysplasia's Disease Ontology ID is recorded as DOID:0060288^[11].
• omodysplasia's Orphanet ID is recorded as 2733^[12].
• omodysplasia's health specialty is recorded as medical genetics^[13].
• omodysplasia's genetic association is recorded as GPC6^[14].
• omodysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060288^[15].
• omodysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0060288^[16].
• omodysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2733^[17].
• omodysplasia's UMLS CUI is recorded as C2750355^[18].
• omodysplasia's UMLS CUI is recorded as C1850318^[19].
• omodysplasia's ICD-10-CM is recorded as Q78.8^[20].
• omodysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine^[21].
• omodysplasia's Mondo ID is recorded as MONDO_0017136^[22].