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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