Disease #04116 (MCOPCB14 (microphthalmia, syndromic, type 14 (MCOPCB-14)), OMIM:615877)

Official abbreviation MCOPCB14
Name microphthalmia, syndromic, type 14 (MCOPCB-14)
OMIM ID 615877
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MAB21L2
Associated tissues -
Disease features -
Remarks -