autosomal recessive limb-girdle muscular dystrophy type 2F Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive limb-girdle muscular dystrophy type 2F (DOID:0110280)
Alliance: disease page
Synonyms: delta-sarcoglycanopathy; LGMD2F; limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
Alt IDs: OMIM:601287, ICD10CM:G71.0, ORDO:219
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the sarcoglycan-delta gene (SGCD).

Disease References using Mouse Models (7)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Sgcdtm1Kcam/Sgcdtm1Kcam	involves: 129S1/Sv * 129X1/SvJ	J:57107	View
Sgcdtm1Mcn/Sgcdtm1Mcn	B6.129-Sgcd^tm1Mcn/J	J:250485	View
Sgcdtm1Mcn/Sgcdtm1Mcn	involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ	J:76730	View