arthrogryposis multiplex congenita

Summary

arthrogryposis multiplex congenita is a developmental defect during embryogenesis^[1].

Key Facts

• arthrogryposis multiplex congenita's instance of is recorded as developmental defect during embryogenesis^[2].
• arthrogryposis multiplex congenita's instance of is recorded as class of disease^[3].
• arthrogryposis multiplex congenita's subclass of is recorded as arthrogryposis^[4].
• arthrogryposis multiplex congenita's MeSH descriptor ID is recorded as C536613^[5].
• arthrogryposis multiplex congenita's KEGG ID is recorded as H02299^[6].
• arthrogryposis multiplex congenita's Disease Ontology ID is recorded as DOID:0080954^[7].
• arthrogryposis multiplex congenita's Orphanet ID is recorded as 1037^[8].
• arthrogryposis multiplex congenita's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1037^[9].
• arthrogryposis multiplex congenita's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080954^[10].
• arthrogryposis multiplex congenita's exact match is recorded as http://identifiers.org/doid/DOID:0080954^[11].
• arthrogryposis multiplex congenita's UMLS CUI is recorded as C2931264^[12].
• arthrogryposis multiplex congenita's ICD-10-CM is recorded as Q74.3^[13].
• arthrogryposis multiplex congenita's GARD rare disease ID is recorded as 777^[14].
• arthrogryposis multiplex congenita's Mondo ID is recorded as MONDO_0015168^[15].
• arthrogryposis multiplex congenita's ICD-11 ID is recorded as LD26.41^[16].
• arthrogryposis multiplex congenita's ICD-11 ID is recorded as 1930990330^[17].