Matches in Wikidata for { <http://www.wikidata.org/entity/Q66084704> ?p ?o ?g. }
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- Q66084704 description "hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36" @default.
- Q66084704 name "hyperprolinemia type 2" @default.
- Q66084704 type Item @default.
- Q66084704 label "hyperprolinemia type 2" @default.
- Q66084704 altLabel "HYRPRO2" @default.
- Q66084704 altLabel "hyperprolinemia type II" @default.
- Q66084704 prefLabel "hyperprolinemia type 2" @default.
- Q66084704 P11430 Q66084704-d33aae7e-472a-a812-e446-73e11e35de45 @default.
- Q66084704 P1550 Q66084704-455A1AD0-1988-401C-A3A9-996E62771371 @default.
- Q66084704 P279 Q66084704-3505C7EE-8EDB-4753-8A52-B255C1126BDC @default.
- Q66084704 P279 Q66084704-49D4AF0C-B8D4-478E-910A-F00876A3BACE @default.
- Q66084704 P2888 Q66084704-309CEA01-521D-45F6-9C3C-4E67C7F9B82A @default.
- Q66084704 P2888 Q66084704-CE7F1195-2CC3-4079-8237-0BDBAE1CAED4 @default.
- Q66084704 P31 Q66084704-A40D10AA-524C-4293-BF7A-46503DB4F6B5 @default.
- Q66084704 P4317 Q66084704-71F5727F-0C68-4DAB-9941-7DA50D809E39 @default.
- Q66084704 P492 Q66084704-4EEA322F-7FB4-4B4B-AFEF-7C9BCB893240 @default.
- Q66084704 P5008 Q66084704-E99E8C4E-1CCB-4554-8F2D-139EEB28C3ED @default.
- Q66084704 P5270 Q66084704-1E7670CB-C171-435E-B065-8CD21CE664DF @default.
- Q66084704 P699 Q66084704-018E7506-11F1-4C6A-B88C-A8288332202A @default.
- Q66084704 P5270 MONDO_0009401 @default.
- Q66084704 P699 DOID_DOID:0080543 @default.
- Q66084704 P11430 "DI-01783" @default.
- Q66084704 P1550 "79101" @default.
- Q66084704 P279 Q10267817 @default.
- Q66084704 P279 Q13637044 @default.
- Q66084704 P2888 DOID:0080543 @default.
- Q66084704 P2888 DOID_0080543 @default.
- Q66084704 P31 Q112193867 @default.
- Q66084704 P4317 "6710" @default.
- Q66084704 P492 "239510" @default.
- Q66084704 P5008 Q4099686 @default.
- Q66084704 P5270 "MONDO_0009401" @default.
- Q66084704 P699 "DOID:0080543" @default.