Disease #04562 (NEM10 (myopathy, nemaline, type 10 (NEM-10)), OMIM:616165)

Official abbreviation NEM10
Name myopathy, nemaline, type 10 (NEM-10)
OMIM ID 616165
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LMOD3
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00424787 - Segarra-Casas 2022, submitted - F yes Spain - - - - - NEM10 HP:0001270, HP:0002359, HP:0030319, HP:0003690, HP:0003798 - LMOD3 1 1 Alba Segarra Casas
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