Disease #00021 (DFNX1 (deafness, X-linked, type 1 (DFNX-1)), OMIM:304500)

Official abbreviation DFNX1
Name deafness, X-linked, type 1 (DFNX-1)
OMIM ID 304500
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PRPS1
Associated tissues -
Disease features -
Remarks -


Individuals

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00266241 - Mercati et al 2019 submitted - M - - - - - - - DFNX1 - PRPS1 PRPS1 1 1 Laurence Jonard
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