acheiropody
Human disease
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acheiropody
Summary
acheiropody is a developmental defect during embryogenesis[1]. acheiropody has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- acheiropody's instance of is recorded as developmental defect during embryogenesis[3].
- acheiropody's instance of is recorded as rare disease[4].
- acheiropody's instance of is recorded as class of disease[5].
- acheiropody is a type of osteochondrodysplasia[6].
- acheiropody is a type of amelia[7].
- acheiropody is a type of non-syndromic terminal limb defects[8].
- acheiropody is a type of autosomal recessive disease[9].
- acheiropody's health specialty is recorded as medical genetics[10].
- acheiropody's genetic association is recorded as LMBR1[11].
- acheiropody's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050603[12].
- acheiropody's exact match is recorded as http://identifiers.org/doid/DOID:0050603[13].
- acheiropody's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_931[14].
- acheiropody's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
acheiropody has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] acheiropody is known by 6 alternative names across languages and contexts.[16]