Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

OCULAR PIGMENT DISPERSION WITH OR WITHOUT GLAUCOMA

Synonyms

PDS

ID

http://purl.bioontology.org/ontology/OMIM/600510

altLabel

PDS

GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME

GLAUCOMA, PIGMENT-DISPERSION TYPE

GPDS1

OPDG

PIGMENT DISPERSION SYNDROME

cui

C1271398

Gene Locus

7q35-q36

Gene Symbol

OPDG

GPDS1

PDS1

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU036427

http://purl.bioontology.org/ontology/OMIM/MTHU075760

http://purl.bioontology.org/ontology/OMIM/MTHU075761

http://purl.bioontology.org/ontology/OMIM/MTHU075762

http://purl.bioontology.org/ontology/OMIM/MTHU057641

http://purl.bioontology.org/ontology/OMIM/MTHU042979

MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.

notation

600510

OMIM Entry Type

5

OMIM MimType Value

perc

prefLabel

OCULAR PIGMENT DISPERSION WITH OR WITHOUT GLAUCOMA

Scope Statement

Age at diagnosis ranged from the 2nd to 4th decade of life [MISCELLANEOUS]

Based on 28 affected individuals from 4 families of Irish ancestry with OPDG mapping to 7q35-36 [MISCELLANEOUS]

tui

T047

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