osteogenesis imperfecta type 11

Summary

osteogenesis imperfecta type 11 is a rare disease^[1].

Key Facts

• osteogenesis imperfecta type 11's instance of is recorded as rare disease^[2].
• osteogenesis imperfecta type 11's instance of is recorded as class of disease^[3].
• osteogenesis imperfecta type 11's subclass of is recorded as osteogenesis imperfecta^[4].
• osteogenesis imperfecta type 11's subclass of is recorded as genetic disease^[5].
• osteogenesis imperfecta type 11's subclass of is recorded as autosomal recessive disease^[6].
• osteogenesis imperfecta type 11's OMIM ID is recorded as 610968^[7].
• osteogenesis imperfecta type 11's Disease Ontology ID is recorded as DOID:0110351^[8].
• osteogenesis imperfecta type 11's Orphanet ID is recorded as 216812^[9].
• osteogenesis imperfecta type 11's Orphanet ID is recorded as 216820^[10].
• osteogenesis imperfecta type 11's health specialty is recorded as medical genetics^[11].
• osteogenesis imperfecta type 11's genetic association is recorded as FKBP10^[12].
• osteogenesis imperfecta type 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110351^[13].
• osteogenesis imperfecta type 11's exact match is recorded as http://identifiers.org/doid/DOID:0110351^[14].
• osteogenesis imperfecta type 11's UMLS CUI is recorded as C3151218^[15].
• osteogenesis imperfecta type 11's UMLS CUI is recorded as C0268362^[16].
• osteogenesis imperfecta type 11's UMLS CUI is recorded as C0268363^[17].
• osteogenesis imperfecta type 11's ICD-10-CM is recorded as Q78.0^[18].
• osteogenesis imperfecta type 11's on focus list of Wikimedia project is recorded as WikiProject Medicine^[19].
• osteogenesis imperfecta type 11's Mondo ID is recorded as MONDO_0012592^[20].
• osteogenesis imperfecta type 11's UniProt disease ID is recorded as DI-03069^[21].