Acrocephalopolydactyly
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Acrocephalopolydactyly
Summary
Acrocephalopolydactyly is a hereditary disorder[1].
Key Facts
- Acrocephalopolydactyly's instance of is recorded as hereditary disorder[2].
- Acrocephalopolydactyly's instance of is recorded as developmental defect during embryogenesis[3].
- Acrocephalopolydactyly's instance of is recorded as class of disease[4].
- Acrocephalopolydactyly's subclass of is recorded as syndromic craniosynostosis[5].
- Acrocephalopolydactyly's MeSH descriptor ID is recorded as C573722[6].
- Acrocephalopolydactyly's OMIM ID is recorded as 200995[7].
- Acrocephalopolydactyly's Orphanet ID is recorded as 221054[8].
- Acrocephalopolydactyly's different from is recorded as Griscelli syndrome type 1[9].
- Acrocephalopolydactyly's Google Knowledge Graph ID is recorded as /g/11bbmk2fsr[10].
- Acrocephalopolydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_221054[11].
- Acrocephalopolydactyly's UMLS CUI is recorded as C3495588[12].
- Acrocephalopolydactyly's UMLS CUI is recorded as C1860157[13].
- Acrocephalopolydactyly's ICD-10-CM is recorded as Q87.0[14].
- Acrocephalopolydactyly's GARD rare disease ID is recorded as 2096[15].
- Acrocephalopolydactyly's Mondo ID is recorded as MONDO_0008709[16].
- Acrocephalopolydactyly's UniProt disease ID is recorded as DI-01519[17].