Search Ontology:
Human Disease
autosomal recessive centronuclear myopathy
- Term ID
- DOID:0111216
- Synonyms
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- AR-CNM
- Definition
- A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348
- References
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- GARD:12718
- ORDO:169186
- Ontology
- Human Disease ( DOID:0111216 )
- is a type of
-
- has subtype
-
Other Pages
Genes Involved
Zebrafish Models
Fish | Conditions | Disease | Citation |
---|---|---|---|
spegahsc191/hsc191; spegbhsc192/hsc192 (AB) | standard conditions | autosomal recessive centronuclear myopathy | Espinosa et al., 2022 |
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