Myopia 26, X-linked, female-limited(MYP26)

MedGen UID:: 1618364
•Concept ID:: C4538795
•: Disease or Syndrome

Synonyms:	MYOPIA 26, X-LINKED, FEMALE-LIMITED; MYP26

Gene (location): Gene(s) directly associated with this condition or phenotype.	ARR3 (Xq13.1)

Monarch Initiative:	MONDO:0049221
OMIM®:	301010

Definition

X-linked myopia-26 is characterized by female-limited early-onset high myopia. The fundus of affected individuals shows a tigroid appearance, and there is a temporal crescent of the optic nerve head (Xiao et al., 2016). For a discussion of genetic heterogeneity of myopia, see 160700. [from OMIM]

Clinical features

From HPO

High myopia

MedGen UID:: 78759
•Concept ID:: C0271183
•: Disease or Syndrome

A severe form of myopia with greater than -6.00 diopters.

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Abnormality of the eye
- High myopia

Recent clinical studies

Clinical prediction guides

Myopia-26, the female-limited form of early-onset high myopia, occurring in a European family.

Széll N, Fehér T, Maróti Z, Kalmár T, Latinovics D, Nagy I, Orosz ZZ, Janáky M, Facskó A, Sohajda Z
Orphanet J Rare Dis 2021 Jan 22;16(1):45. doi: 10.1186/s13023-021-01673-z. PMID: 33482870 Free PMC Article

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Myopia 26, X-linked, female-limited(MYP26)

Definition

Clinical features

Recent clinical studies

Clinical prediction guides

Supplemental Content

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Genetic Testing Registry

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