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Microphthalmia/coloboma 11(MCOPCB11)

MedGen UID:
1052456
Concept ID:
CN376899
Disease or Syndrome
Synonym: MCOPCB11
 
Gene (location): FZD5 (2q33.3)
 
Monarch Initiative: MONDO:0958239
OMIM®: 620731

Definition

Microphthalmia/coloboma-11 (MCOPCB11) is characterized by ocular coloboma and related phenotypes such as inferior chorioretinal hypoplasia and/or optic disc hypoplasia, with occasional microphthalmia or high myopia. Incomplete penetrance as well as intrafamilial and intraindividual phenotypic variability have been observed (Liu et al., 2016; Aubert-Mucca et al., 2021; Jiang et al., 2021; Holt et al., 2022). For a discussion of genetic heterogeneity of colobomatous microphthalmia, see MCOPCB1 (300345). [from OMIM]

Recent clinical studies

Etiology

Nayak A, Dave TV, Ali MJ, Tiwari A
Orbit 2020 Jun;39(3):155-159. Epub 2019 Jul 3 doi: 10.1080/01676830.2019.1634105. PMID: 31267812

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