RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:
autosomal recessive limb-girdle muscular dystrophy type 2I
An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin-related protein (FKRP) on chromosome 19q13.3. (DO)
Synonyms:
exact_synonym:
LGMD2I; LGMDR9; MDDGC5; autosomal recessive limb-girdle muscular dystrophy 9; limb-girdle muscular dystrophy due to FKRP deficiency; limb-girdle muscular dystrophy, type 2I; limb-girdle muscular dystrophy-dystroglycanopathy, FRKP-related; limb-girdle muscular dystrophy-dystroglycanopathy, type C5; muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5