Human Phenotype Ontology

Last uploaded: February 24, 2022
Preferred Name

Pigmentary retinopathy

Synonyms

Retinal pigment clumping

Retinal pigmentary degeneration

Pigmentary retinal deposits

Retinal pigmentary clumping

Definitions

An abnormality of the retina characterized by pigment deposition. It is typically associated with migration and proliferation of macrophages or retinal pigment epithelial cells into the retina; melanin from these cells causes the pigmentary changes. Pigmentary retinopathy is a common final pathway of many retinal conditions and is often associated with visual loss.

ID

http://purl.obolibrary.org/obo/HP_0000580

database_cross_reference

UMLS:C0035334

SNOMEDCT_US:28835009

MSH:D012174

definition

An abnormality of the retina characterized by pigment deposition. It is typically associated with migration and proliferation of macrophages or retinal pigment epithelial cells into the retina; melanin from these cells causes the pigmentary changes. Pigmentary retinopathy is a common final pathway of many retinal conditions and is often associated with visual loss.

has_alternative_id

HP:0007934

HP:0007702

HP:0007821

HP:0008010

HP:0007961

HP:0007869

HP:0007852

HP:0001146

has_exact_synonym

Retinal pigment clumping

Retinal pigmentary degeneration

Pigmentary retinal deposits

Retinal pigmentary clumping

has_obo_namespace

human_phenotype

id

HP:0000580

label

Pigmentary retinopathy

notation

HP:0000580

prefLabel

Pigmentary retinopathy

treeView

http://purl.obolibrary.org/obo/HP_0007703

subClassOf

http://purl.obolibrary.org/obo/HP_0007703

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http://purl.obolibrary.org/obo/HP_0000580 Human Disease Ontology 123 LOOM
http://purl.obolibrary.org/obo/HP_0000580 Human Disease Ontology 123 SAME_URI
http://purl.bioontology.org/ontology/OMIM/MTHU000153 Online Mendelian Inheritance in Man LOOM