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ENMicrocoria, Congenital (MCOR)
Alias:
Congenital Miosis
Congenital Microcoria
Miosis, Congenital
Chromosome 13q32 Deletion Syndrome
Mcor
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Microcoria, Congenital, also known as congenital miosis, is related to pierson syndrome and spastic ataxia 7, autosomal dominant. An important gene associated with Microcoria, Congenital is MCOR (Microcoria, Congenital). Affiliated tissues include eye, and related phenotypes are iris hypopigmentation and hypoplastic iris stroma
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MALACARDS
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