ZFIN Human Disease: nemaline myopathy

OBO ID: DOID:3191

Term Name:	nemaline myopathy		Search Ontology:
Synonyms:	Nemaline body disease nemaline rod myopathy rod body disease rod myopathy
Definition:	A congenital myopathy characterized by generally non-progressive muscle weakness of varying severity and problems with the tone and contraction of skeletal muscles. The muscle cells contain abnormal clumps of threadlike material called nemaline bodies. (4)
References:	GARD:12033 ICD10CM:G71.21 MESH:D017696 OMIM:PS161800 ORDO:607 SNOMEDCT_US_2023_03_01:75072002 UMLS_CUI:C0206157
Ontology:	Human Disease ( DOID:3191 )

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
neb^{hu2849/hu2849}	standard conditions	Qiu et al., 2019
neb^sa906/sa906	standard conditions	Sztal et al., 2018
AB + MO1-lmod3 + MO2-lmod3	standard conditions	Yuen et al., 2014
WT + MO1-actc1b	standard conditions	Sztal et al., 2015
WT + MO1-neb	standard conditions	Sztal et al., 2015
WT + MO1-neb + MO2-neb	standard conditions	Sztal et al., 2015
WT + MO2-actc1b	standard conditions	Sztal et al., 2015
WT + MO2-neb	standard conditions	Sztal et al., 2015
mnu3Tg	standard conditions	Sztal et al., 2016
mnu3Tg; mnu5Tg	standard conditions	(2)
mnu4Tg; mnu5Tg	standard conditions	Sztal et al., 2015

PHENOTYPE No data available

CITATIONS (9)