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loading...| Preferred Name | Weill-Marchesani syndrome 2 | |
| Synonyms |
WMS2 |
|
| Definitions |
(WMS2) - A rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, and eye abnormalities including microspherophakia, ectopia lentis, severe myopia and glaucoma. |
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| ID |
http://identifiers.org/omim/608328 |
|
| altLabel |
WMS2 |
|
| definition |
(WMS2) - A rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, and eye abnormalities including microspherophakia, ectopia lentis, severe myopia and glaucoma. |
|
| id |
OMIM:608328 |
|
| notation |
OMIM:608328 |
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| prefLabel |
Weill-Marchesani syndrome 2 |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://identifiers.org/omim/608328 | REXO | SAME_URI | |
| http://identifiers.org/omim/608328 | RETO | SAME_URI | |
| http://identifiers.org/omim/608328 | REXO | LOOM | |
| http://identifiers.org/omim/608328 | RETO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/608328 | OMIM | LOOM | |
| http://purl.obolibrary.org/obo/OMIM_608328 | CCO | LOOM |