Disease #02541 (NEM5 (myopathy, nemaline, type 5 (NEM-5)), OMIM:605355)

Official abbreviation NEM5
Name myopathy, nemaline, type 5 (NEM-5)
OMIM ID 605355
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 TNNT1
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

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00472224 - Verebi et al. (submitted) - F - France - - - - - NEM5 Muscle weakness, Generalized limb muscle atrophy - TNNT1 1 1 Camille Verebi
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