Disease #02841 (NEM4 (myopathy, nemaline, type 4 (NEM-4)), OMIM:609285)

Official abbreviation NEM4
Name myopathy, nemaline, type 4 (NEM-4)
OMIM ID 609285
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 TPM2
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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00472214 - Verebi et al. (sobmitted) - M - France - - - - - NEM4 Myopathy, Congenital contracture, Spinal rigidity - TPM2 1 1 Camille Verebi
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