acrocapitofemoral dysplasia
Human disease
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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 is a type of osteochondrodysplasia[5].
- acrocapitofemoral dysplasia is a type of acromelic dysplasia[6].
- acrocapitofemoral dysplasia is a type of autosomal recessive disease[7].
- acrocapitofemoral dysplasia's genetic association is recorded as IHH[8].
- acrocapitofemoral dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050604[9].
- acrocapitofemoral dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0050604[10].
- acrocapitofemoral dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_63446[11].
- acrocapitofemoral dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].