Jump to:
loading...| Preferred Name | Weill-Marchesani syndrome 1 | |
| Synonyms |
WMS1 |
|
| Definitions |
(WMS1) - A rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, and eye abnormalities including microspherophakia, ectopia lentis, severe myopia and glaucoma. |
|
| ID |
http://identifiers.org/omim/277600 |
|
| altLabel |
WMS1 |
|
| definition |
(WMS1) - 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:277600 |
|
| notation |
OMIM:277600 |
|
| prefLabel |
Weill-Marchesani syndrome 1 |
|
| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://identifiers.org/omim/277600 | REXO | SAME_URI | |
| http://identifiers.org/omim/277600 | GEXO | SAME_URI | |
| http://identifiers.org/omim/277600 | REXO | LOOM | |
| http://identifiers.org/omim/277600 | GEXO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0010194 | MONDO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0010194 | DOVES | LOOM | |
| http://purl.obolibrary.org/obo/OMIM_277600 | CCO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/277600 | OMIM | LOOM |