Disease #00023 (DFNX-4 (deafness, X-linked, type 4 (DFNX-4)), OMIM:300066)

Official abbreviation DFNX-4
Name deafness, X-linked, type 4 (DFNX-4)
OMIM ID 300066
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 0
Associated with 1 gene SMPX
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00000133 - - These individuals have profound X-linked hearing loss M ? Canada Newfoundland, Caucasian - - - - DFNX-4 - SKI, SMPX SMPX 1 6 Terry-Lynn Young
00000134 - - These individuals have variable X-linked hearing loss F ? Canada Newfoundland, Caucasian - - - - DFNX-4 - SMPX SMPX 1 3 Terry-Lynn Young
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