aurocephalosyndactyly
human disease
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aurocephalosyndactyly
Summary
aurocephalosyndactyly is a class of disease[1].
Key Facts
- aurocephalosyndactyly's instance of is recorded as class of disease[2].
- aurocephalosyndactyly's subclass of is recorded as disease[3].
- aurocephalosyndactyly's said to be the same as is recorded as Saethre-Chotzen syndrome[4].
- aurocephalosyndactyly's MeSH descriptor ID is recorded as C566235[5].
- aurocephalosyndactyly's OMIM ID is recorded as 109050[6].
- aurocephalosyndactyly's Orphanet ID is recorded as 1219[7].
- aurocephalosyndactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1219[8].
- aurocephalosyndactyly's UMLS CUI is recorded as C1862380[9].
- aurocephalosyndactyly's GARD rare disease ID is recorded as 9218[10].
- aurocephalosyndactyly's Mondo ID is recorded as MONDO_0007178[11].