acrocapitofemoral dysplasia

Summary

acrocapitofemoral dysplasia is a developmental defect during embryogenesis^[1].

Key Facts

• acrocapitofemoral dysplasia's instance of is recorded as developmental defect during embryogenesis^[2].
• acrocapitofemoral dysplasia's instance of is recorded as rare disease^[3].
• acrocapitofemoral dysplasia's instance of is recorded as class of disease^[4].
• acrocapitofemoral dysplasia's subclass of is recorded as osteochondrodysplasia^[5].
• acrocapitofemoral dysplasia's subclass of is recorded as acromelic dysplasia^[6].
• acrocapitofemoral dysplasia's subclass of is recorded as autosomal recessive disease^[7].
• acrocapitofemoral dysplasia's MeSH descriptor ID is recorded as C564334^[8].
• acrocapitofemoral dysplasia's OMIM ID is recorded as 607778^[9].
• acrocapitofemoral dysplasia's KEGG ID is recorded as H00675^[10].
• acrocapitofemoral dysplasia's Disease Ontology ID is recorded as DOID:0050604^[11].
• acrocapitofemoral dysplasia's Orphanet ID is recorded as 63446^[12].
• acrocapitofemoral dysplasia's genetic association is recorded as IHH^[13].
• acrocapitofemoral dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050604^[14].
• acrocapitofemoral dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0050604^[15].
• acrocapitofemoral dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_63446^[16].
• acrocapitofemoral dysplasia's UMLS CUI is recorded as C1843096^[17].
• acrocapitofemoral dysplasia's ICD-10-CM is recorded as Q78.8^[18].
• acrocapitofemoral dysplasia's GARD rare disease ID is recorded as 10605^[19].
• acrocapitofemoral dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine^[20].
• acrocapitofemoral dysplasia's Mondo ID is recorded as MONDO_0011907^[21].
• acrocapitofemoral dysplasia's UniProt disease ID is recorded as DI-00026^[22].