Details of Disease

General Information of Disease (ID: DISI49GW)

Disease Name Polydactyly, postaxial, type a10
Synonyms PAPA10; POLYDACTYLY, POSTAXIAL, TYPE A10
Disease Hierarchy
DIS085OV: Postaxial polydactyly
DISI49GW: Polydactyly, postaxial, type a10
Disease Identifiers
MONDO ID
MONDO_0032785
UMLS CUI
C5193129
OMIM ID
618498
MedGen ID
1676955

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
KIAA0825 OTANX32T Strong Autosomal recessive [1]
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References

1 Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay. Eur J Hum Genet. 2016 Nov;24(11):1622-1626. doi: 10.1038/ejhg.2016.64. Epub 2016 Jul 6.