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loading...| Preferred Name |
Sclerocornea |
| ID |
http://purl.bioontology.org/ontology/MESH/C565209 |
| cui |
C1853235 |
| Has mapping qualifier | |
| HM |
D003315/Q000002 D003316 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20121105 |
| MeSH Frequency |
35 |
| MMR |
20160929 |
| notation |
C565209 |
| prefLabel |
Sclerocornea |
| SC |
3 |
| Scope Statement |
A hereditary abnormality characterized by scleralization or opacity of the peripheral or entire cornea. OMIM: 181700 |
| TERMUI |
T806355 |
| TH |
OMIM (2013) |
| tui |
T047 |
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