retinal diseases

Preferred Label : retinal diseases;

MeSH definition : Diseases involving the RETINA.;

MeSH synonym : retinal disease; disease, retinal; diseases, retinal;

MeSH annotation : inflammatory disease RETINITIS or specifics;

Details

Origin ID

D012164;

UMLS CUI

C0035309;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Abnormal retinal morphology [HPO term]
- Background retinopathy and retinal vascular changes [ICD-10 Sub-category (who)]
- Disorders of the retina [Bloc CIM-11]
- Other retinal disorders [ICD-9 code]
- Other retinal disorders [ICD-9 code]
- Other retinal disorders [ICD-10 category (who)]
- Retinopathies [PASCAL theme]
- Retinopathy, CTCAE [NCIt concept]
- retinal disease [DO Concept]
- retinitis, nos [SNOMED Notion]
CISMeF manual mappings
- retinopathy [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Certain specified retinal disorders [ICD-11 Category]
- Disorder retinal [MedDRA LLT]
- RETINAL DISORDER [WHO-ART High Level Term]
- RETINOPATHY [WHO-ART Included Term]
- Retinal Disorder [NCIt concept]
- Retinal disorder [MedDRA Preferred Term]
- Retinal disorder (disorder) [SNOMED CT concept]
- Retinal disorder NOS [MedDRA LLT]
- Retinal disorders (SMQ) [MedDRA Standard Query]
- Retinopathy [PASCAL descriptor]
- Retinopathy [ICD-11 Category]
- Retinopathy [HPO term]
- Retinopathy [MedDRA Preferred Term]
- Retinopathy [NCIt concept]
- Retinopathy [HRDO Sign]
- Retinopathy (disorder) [Inactive SNOMED CT concept]
- Retinopathy NOS [MedDRA LLT]
- Unspecified retinal disorder [ICD-9 code]
- Unspecified retinal disorder [ICD-10 Sub-category]
- retina disorder [Disease (Nov.)]
- retinal disorder, nos [SNOMED Notion]
- retinal disorders [MedlinePlus Topic]
DO Cross reference
- retinal disease [DO Concept]
HPO term
- Abnormal retinal morphology [HPO term]
- Retinopathy [HPO term]
MedlinePlus topic(s)
- retinal disorders [MedlinePlus Topic]
Record concept(s)
- retinal diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- Al Gazali Sabrinathan Nair syndrome [MeSH Supplementary Concept]
- FLOTCH syndrome [MeSH Supplementary Concept]
- ausems Wittebol-Post hennekam syndrome [MeSH Supplementary Concept]
- bestrophinopathy [MeSH Supplementary Concept]
- bietti crystalline dystrophy [MeSH Supplementary Concept]
- bothnia retinal dystrophy [MeSH Supplementary Concept]
- cerebroretinal microangiopathy with calcifications and cysts [MeSH Supplementary Concept]
- exudative vitreoretinopathy 4 [MeSH Supplementary Concept]
- exudative vitreoretinopathy 5 [MeSH Supplementary Concept]
- fleck retina, familial benign [MeSH Supplementary Concept]
- fundus albipunctatus [MeSH Supplementary Concept]
- grouped pigmentation of the macula [MeSH Supplementary Concept]
- iris hypoplasia and glaucoma [MeSH Supplementary Concept]
- microcephaly with chorioretinopathy, autosomal dominant [MeSH Supplementary Concept]
- microcephaly with chorioretinopathy, autosomal recessive [MeSH Supplementary Concept]
- oculomelic amyoplasia [MeSH Supplementary Concept]
- rambaud galian syndrome [MeSH Supplementary Concept]
- ramos arroyo clark syndrome [MeSH Supplementary Concept]
- retinal aplasia [MeSH Supplementary Concept]
- retinal nonattachment, nonsyndromic congenital [MeSH Supplementary Concept]
- roifman syndrome [MeSH Supplementary Concept]
- stickler syndrome, autosomal recessive, COL9A1-Related [MeSH Supplementary Concept]
- vasculopathy, retinal, with cerebral leukodystrophy [MeSH Supplementary Concept]
- vitreoretinopathy with phalangeal epiphyseal dysplasia [MeSH Supplementary Concept]
See also
- color vision defects [MeSH Descriptor]
See also (suggested by CISMeF)
- retina [MeSH Descriptor]
- retinitis [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Certain specified retinal disorders [ICD-11 Category]
- Disorder retinal [MedDRA LLT]
- RETINAL DISORDER [WHO-ART High Level Term]
- RETINOPATHY [WHO-ART Included Term]
- Retinal Disorder [NCIt concept]
- Retinal disorder [MedDRA Preferred Term]
- Retinal disorder (disorder) [SNOMED CT concept]
- Retinal disorder NOS [MedDRA LLT]
- Retinopathy [MedDRA Preferred Term]
- Retinopathy [HPO term]
- Retinopathy [HRDO Sign]
- Retinopathy [PASCAL descriptor]
- Retinopathy [NCIt concept]
- Retinopathy (disorder) [Inactive SNOMED CT concept]
- Retinopathy NOS [MedDRA LLT]
- Unspecified retinal disorder [ICD-9 code]
- Unspecified retinal disorder [MedDRA LLT]
- Unspecified retinal disorder [ICD-10 Sub-category]
- retinal disease [DO Concept]
- retinal disorder, nos [SNOMED Notion]
- retinal disorders [MedlinePlus Topic]
- retinopathy [ICPC-2 Rubric]

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