loading...| Preferred Name |
Pigmentary Retinopathy |
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| Synonyms |
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| 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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| ID |
http://www.phoc.org.cn/pmo/class/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 |
|
| 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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| equivalentClass |
http://www.phoc.org.cn/pmo/class/PMO_00006723 |
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| label |
Pigmentary Retinopathy |
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| MCID |
MC00011322 |
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| PMOID |
PMO:00006662 |
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| prefixIRI |
pmo:PMO_00006662 |
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| prefLabel |
Pigmentary Retinopathy |
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| 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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| Tree Number |
T3.18.1.6.2.9.14.1 |
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| subClassOf |
http://www.phoc.org.cn/pmo/class/PMO_00037136 http://www.phoc.org.cn/pmo/class/PMO_00006717 http://www.phoc.org.cn/pmo/class/PMO_00006661 |