Matches in Wikidata for { <http://www.wikidata.org/entity/Q66084932> ?p ?o ?g. }
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- Q66084932 description "A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in POMGNT1 on 1p34.1." @default.
- Q66084932 name "congenital muscular dystrophy-dystroglycanopathy type A3" @default.
- Q66084932 type Item @default.
- Q66084932 label "congenital muscular dystrophy-dystroglycanopathy type A3" @default.
- Q66084932 altLabel "MDDGA3" @default.
- Q66084932 altLabel "Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related" @default.
- Q66084932 altLabel "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3" @default.
- Q66084932 prefLabel "congenital muscular dystrophy-dystroglycanopathy type A3" @default.
- Q66084932 P279 Q66084932-ECCB3965-D037-42C2-B3CA-AE51BA455124 @default.
- Q66084932 P2888 Q66084932-B01FFF75-F20D-4DB5-8881-E084962854E3 @default.
- Q66084932 P2888 Q66084932-E964944C-A8EC-4C04-A5F9-53C2FB08BA76 @default.
- Q66084932 P31 Q66084932-F7DDEB10-04E8-458D-A703-A57CE8A67244 @default.
- Q66084932 P492 Q66084932-D6630F3B-83A9-4CC8-9574-7E94CE41F6C0 @default.
- Q66084932 P5008 Q66084932-96C501A4-AA47-4C4F-BAA2-93681752A28B @default.
- Q66084932 P699 Q66084932-F819092D-A82B-4014-9F5B-6D2DAAF8B44C @default.
- Q66084932 P699 DOID_DOID:0111236 @default.
- Q66084932 P279 Q66084925 @default.
- Q66084932 P2888 DOID:0111236 @default.
- Q66084932 P2888 DOID_0111236 @default.
- Q66084932 P31 Q112193867 @default.
- Q66084932 P492 "253280" @default.
- Q66084932 P5008 Q4099686 @default.
- Q66084932 P699 "DOID:0111236" @default.