Disease #06201 (CMYO16;MYOTREM (myopathy, congenital, type 16), OMIM:618524)

Official abbreviation CMYO16;MYOTREM
Name myopathy, congenital, type 16
OMIM ID 618524
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MYBPC1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2026-02-06 10:11:07 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00472256 - Verebi et al. (submitted) - F - France - - - - - CMYO16;MYOTREM 0003198: Myopathy, 0009062: Axial hypotonia in infants, 0012389: Appendicular hypotonia, 0002174: Postural tremor, 0002322: Resting tremor, 0007089: Faciolingual fasciculations - MYBPC1 1 1 Camille Verebi
00472257 - Verebi et al. (submitted) - M - France - - - - - CMYO16;MYOTREM 0001337: Tremor, 0009020: Exercise-induced muscle fatigue, 0002315: Headache, 0002380: Fasciculations - MYBPC1 1 1 Camille Verebi
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