acromicric dysplasia
Acromicric dysplasia is a rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands
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acromicric dysplasia
Summary
acromicric dysplasia is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- acromicric dysplasia's instance of is recorded as developmental defect during embryogenesis[3].
- acromicric dysplasia's instance of is recorded as rare disease[4].
- acromicric dysplasia's instance of is recorded as class of disease[5].
- acromicric dysplasia is a type of osteochondrodysplasia[6].
- acromicric dysplasia is a type of acromelic dysplasia[7].
- acromicric dysplasia's ICD-9-CM is recorded as 756.59[8].
- acromicric dysplasia's genetic association is recorded as FBN1[9].
- acromicric dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_969[10].
- acromicric dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111243[11].
- acromicric dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:0111243[12].
- acromicric dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
acromicric dysplasia is known by 5 alternative names across languages and contexts.[2]