Disease #07093 (CMT1J (Charcot-Marie-Tooth disease, demyelinating, type 1J), OMIM:620111)

Official abbreviation CMT1J
Name Charcot-Marie-Tooth disease, demyelinating, type 1J
OMIM ID 620111
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ITPR3
Associated tissues -
Disease features -
Remarks -
Date created 2024-06-24 17:17:24 +02:00 (CEST)
Date last edited N/A


Individuals

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00474161 365796 - - F no ? (unknown) - - - - - CMT1J Muscle weakness, Positional foot deformity ITPR3 ITPR3 1 1 Andreas Laner
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