Jump to:
loading...| Preferred Name |
Galactosemia II |
|
| Synonyms |
|
|
| Definitions |
(GALCT2): Autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of galactitol in the lenses. |
|
| ID |
http://purl.obolibrary.org/obo/OMIM_230200 |
|
| definition |
(GALCT2): Autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of galactitol in the lenses. |
|
| has_obo_namespace |
cell_cycle_ontology |
|
| id |
OMIM:230200 |
|
| label |
Galactosemia II |
|
| notation |
OMIM:230200 |
|
| prefLabel |
Galactosemia II |
|
| treeView | ||
| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://identifiers.org/omim/230200 | REXO | LOOM | |
| http://identifiers.org/omim/230200 | GEXO | LOOM | |
| http://identifiers.org/omim/230200 | RETO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/230200 | OMIM | LOOM |