Disease #01660 (MLA (microphthalmia, with limb anomalies (MLA, anophthalmia)), OMIM:206920)
| Official abbreviation |
MLA |
| Name |
microphthalmia, with limb anomalies (MLA, anophthalmia) |
| OMIM ID |
206920 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SMOC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
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