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PMO Precision Medicine Ontology
Last uploaded:
December 16, 2020
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| Id | http://www.phoc.org.cn/pmo/class/PMO_00006662
http://www.phoc.org.cn/pmo/class/PMO_00006662
|
|---|---|
| Preferred Name | Pigmentary Retinopathy |
| 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.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
Pigmentary Retinopathy
|
|---|---|
| prefLabel |
Pigmentary Retinopathy
|
| Synonym |
Retinopathy, Pigmentary
RP
Rod Cone Dystrophies
CORD
CRD2
Retinitis pigmentosa (disorder)
Retinitis Pigmentosa [Disease/Finding]
CONE-ROD DYSTROPHY 2
Cone-rod retinal dystrophy
DYSTROPHY, PERIPHERAL TAPETORETINAL
Retinitis Pigmentosa
Cone-rod dystrophy
Pigmentary Retinopathies
Pigmentary retinopathy
CHORIORETINAL HEREDODYSTROPHY
Tapetoretinal Degenerations
Rod-Cone Dystrophies
RETINAL CONE-ROD DYSTROPHY
CORD2
cone rod dystrophy
Pigmentary maculopathy
retinitis pigmentosa (diagnosis)
pericentral pigmentary retinopathy
Rod-Cone Dystrophy
Rod Cone Dystrophy
Tapetoretinal degeneration
Retinopathies, Pigmentary
RCRD2
retinal cone-rod dystrophy 2
RP - Retinitis pigmentosa
Retinitis pigmentosa (RP)
CRD
Retinitis;pigmentosa
cone-rod retinal dystrophy 2
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|
| 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.
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| PMOID |
PMO:00006662
|
| MCID |
MC00011322
|
| prefixIRI |
pmo:PMO_00006662
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| Database_Cross_Reference |
MDR:10054856
DXP:U001673
MTH:NOCODE
CCPSS:0041901
MTHICD9:362.74
ICPC2P:F99053
OMIM:MTHU001509
CSP:1114-9526
MEDCIN:30731
OMIM:604011
HPO:HP:0000547
LCH:U004109
OMIM:MTHU005737
MDR:10038914
ICD10CM:H35.52
NCI:C85045
DO:DOID:10584
OMIM:MTHU030127
SNOMEDCT_US:28835009
CST:RETINAL PIGMENT
COSTAR:U000595
CHV:0000010812
MSH:D012174
SNMI:DA-71906
SNM:D-X030
RCD:X00dw
HPO:HP:0000510
LCH_NW:sh85113336
OMIM:120970
DXP:NOCODE
HPO:HP:0000580
SNOMEDCT_US:155113002
OMIM:MTHU000153
RCD:F4276
OMIM:MTHU000322
DO:DOID:0111005
OMIM:268000
NDFRT:N0000002614
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| Tree Number |
T3.18.1.6.2.9.14.1
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| subClassOf | |
| equivalentClass | |
| type |
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