Current Data About
primary hyperoxaluria type I
| (P31) |
(Q112193867)
|
||||||||||||
| (P279) |
(Q55787328)
(Q7243137)
|
||||||||||||
| (P1692) |
271.8
|
||||||||||||
| (P1748) |
C123212
|
||||||||||||
| (P2293) |
(Q17816233)
|
||||||||||||
| (P2888) |
http://www.orpha.net/ORDO/Orphanet_416
http://www.orpha.net/ORDO/Orphanet_93598 http://purl.obolibrary.org/obo/DOID_0111670
http://identifiers.org/doid/DOID:0111670
|
other details
| aliases |
oxalosis I gylcolytic aciduria serine:pyruvate aminotransferase deficiency HP1 Alanine-Glyoxylate Aminotransferase Deficiency Peroxisomal alanine-glyoxylate aminotransferase deficiency Glycolic aciduria Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency Oxalosis 1 Serine pyruvate aminotransferase deficiency Primary Hyperoxaluria Type I Hepatic Agt Deficiency HYPEROXALURIA, PRIMARY, TYPE I; HP1 Peroxisomal alanine glyoxylate aminotransferase deficiency HYPEROXALURIA, PRIMARY, TYPE I primary hyperoxaluria type 1 |
| description | human disease |
External Links
| (P486) |
C536414
|
| (P492) |
259900
|
| (P699) |
DOID:0111670
|
| (P1550) |
93598
|
| (P2892) |
C0268164
|
| (P4229) |
E74.8
|
| (P4317) |
2835
|
| (P5270) |
MONDO_0009823
|
| (P7329) |
5C51.20
|
| (P7807) |
692812009
|
| (P11430) |
DI-01778
|