acheiropody
Human disease
Facts
9 properties- Instance of
- rare disease, class of disease[6]
- Subclass of
- osteochondrodysplasia, amelia, non-syndromic terminal limb defects, autosomal recessive disease, developmental defect during embryogenesis[7]
- Has phenotype
- abnormality of the metaphysis, Absent radius, Aplasia of the ulna, acheiria, Short humerus, Upper limb phocomelia[14][15][16][17][18][19]
- Health specialty
- medical genetics[9]
- On focus list of Wikimedia project
- WikiProject Medicine[13]
- P14914
- D00931[20]
- Prevalence
- +0.000001[8]
🏷️ Also known as
en ACHP
en Horn-Kolb Syndrome
en Acheiropodia
en acheiropody
en Acheiropody
en ACHEIROPODY; ACHP
en Acheiropody, Brazilian Type
ar انعدام نهايات الأطراف
de Acheiropodie
es Aqueiropodia
fr achéiropodie
tr Akeyropodi
zh 無手足畸形
🔖 Identifiers · 15
- Disease Ontology ID
- DOID:0050603
- DiseasesDB
- 32738
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- ICD-10 ID
- Q74.8
- ICD-10-CM
- Q74.8
- KEGG ID
- H00629
- MeSH descriptor ID
- C536014
- Microsoft Academic ID (discontinued)
- 2779082981
- Mondo ID
- MONDO_0008700
- OMIM ID
- 200500
- Orphanet ID
- 931
Show all 15 identifiers +3
- UMLS CUI
- C0265559
- UniProt disease ID
- DI-01165
- WikiProjectMed ID
- Acheiropodia
🔗 Connections
Subclass of 2
Genetic association 1
Health specialty 1
Instance of 1
On focus list of Wikimedia project 1
← Genetic association 1
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