Disease #02924 (DFNB67 (deafness, autosomal recessive, type 67 (DFNB-67)), OMIM:610265)

Official abbreviation DFNB67
Name deafness, autosomal recessive, type 67 (DFNB-67)
OMIM ID 610265
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene LHFPL5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00152005 - - Article under review F no France Reunion Island 17y - - cochlear implant DFNB67 bilateral profound deafness, walking delay, bilateral vestibular areflexia LHFPL5 LHFPL5 1 1 Justine Lerat
00448501 - - - F yes Pakistan - - - - - DFNB67 - LHFPL5 LHFPL5 1 1 Hina Khan
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