Disease #02924

Official abbreviation DFNB-67
Name deafness, autosomal recessive, type 67 (DFNB-67)
OMIM ID 610265
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LHFPL5
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Individuals

1 entry on 1 page. Showing entry 1.
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00152005 - - Article under review F no France Reunion Island 17y 0 - cochlear implant DFNB-67 bilateral profound deafness, walking delay, bilateral vestibular areflexia LHFPL5 LHFPL5 1 1 Justine Lerat
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