osteoglophonic dwarfism

Summary

osteoglophonic dwarfism is a developmental defect during embryogenesis^[1].

Key Facts

• osteoglophonic dwarfism's instance of is recorded as developmental defect during embryogenesis^[2].
• osteoglophonic dwarfism's instance of is recorded as rare disease^[3].
• osteoglophonic dwarfism's instance of is recorded as class of disease^[4].
• osteoglophonic dwarfism's subclass of is recorded as primary bone dysplasia with disorganized development of skeletal components^[5].
• osteoglophonic dwarfism's subclass of is recorded as autosomal dominant disease^[6].
• osteoglophonic dwarfism's subclass of is recorded as osteochondrodysplasia^[7].
• osteoglophonic dwarfism's MeSH descriptor ID is recorded as C536050^[8].
• osteoglophonic dwarfism's OMIM ID is recorded as 166250^[9].
• osteoglophonic dwarfism's KEGG ID is recorded as H00443^[10].
• osteoglophonic dwarfism's Disease Ontology ID is recorded as DOID:0111532^[11].
• osteoglophonic dwarfism's Orphanet ID is recorded as 2645^[12].
• osteoglophonic dwarfism's genetic association is recorded as FGFR1^[13].
• osteoglophonic dwarfism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2645^[14].
• osteoglophonic dwarfism's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111532^[15].
• osteoglophonic dwarfism's exact match is recorded as http://identifiers.org/doid/DOID:0111532^[16].
• osteoglophonic dwarfism's UMLS CUI is recorded as C0432283^[17].
• osteoglophonic dwarfism's ICD-10-CM is recorded as Q87.1^[18].
• osteoglophonic dwarfism's GARD rare disease ID is recorded as 4142^[19].
• osteoglophonic dwarfism's Mondo ID is recorded as MONDO_0008150^[20].
• osteoglophonic dwarfism's Genetics Home Reference Conditions ID is recorded as osteoglophonic-dysplasia^[21].
• osteoglophonic dwarfism's UniProt disease ID is recorded as DI-02110^[22].