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 |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SMOC1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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