eye abnormalities

Preferred Label : eye abnormalities;

MeSH definition : Congenital absence of or defects in structures of the eye; may also be hereditary.;

MeSH synonym : abnormality, eye; eye abnormality; abnormalities, eye;

MeSH annotation : do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; these are structural abnorm: EYE DISEASES, HEREDITARY is also available;

Details

Origin ID

D005124;

UMLS CUI

C0015393;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [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)
- Congenital eye disorder [MedDRA Preferred Term]
- Congenital malformations of the eye [ICD-11 More detail]
- EYE MALFORMATION [WHO-ART Preferred Term]
- Eye abnormality NOS [MedDRA LLT]
- Eye malformation [MedDRA LLT]
- Malformations of the eye [PASCAL theme]
- eye malformation [BNCI symptom]
Currated CISMeF NLP mapping
- Abnormality of the eye [HPO term]
- EYE ABNORMALITY [WHO-ART Preferred Term]
- Eye abnormality [MedDRA LLT]
- eye abnormality [Disease (Nov.)]
HPO term
- Abnormality of the eye [HPO term]
Mapping VCM hiérarchique
- deformity [VCM modifier]
MeSH Descriptor(s) used for indexing
- eye [MeSH Descriptor]
Record concept(s)
- eye abnormalities [MeSH concept]
Related MeSH Supplementary Concept(s)
- Agenesis of Cerebellar Vermis [MeSH Supplementary Concept]
- Ankyloblepharon filiforme adnatum [MeSH Supplementary Concept]
- Axenfeld-Rieger anomaly with cardiac defects and sensorineural hearing loss [MeSH Supplementary Concept]
- Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities [MeSH Supplementary Concept]
- Axenfeld-Rieger syndrome [MeSH Supplementary Concept]
- Brachymetapody-Anodontia-Hypotrichosis-Albinoidism [MeSH Supplementary Concept]
- Brittle cornea syndrome 1 [MeSH Supplementary Concept]
- CODAS syndrome [MeSH Supplementary Concept]
- FACES syndrome [MeSH Supplementary Concept]
- Goniodysgenesis-Mental Retardation-Short stature syndrome [MeSH Supplementary Concept]
- Hay-Wells syndrome [MeSH Supplementary Concept]
- MOMES syndrome [MeSH Supplementary Concept]
- PHACE association [MeSH Supplementary Concept]
- Schmid-Fraccaro syndrome [MeSH Supplementary Concept]
- ablepharon macrostomia syndrome [MeSH Supplementary Concept]
- anterior segment mesenchymal dysgenesis [MeSH Supplementary Concept]
- asymmetric short stature syndrome [MeSH Supplementary Concept]
- blue diaper syndrome [MeSH Supplementary Concept]
- chemke oliver mallek syndrome [MeSH Supplementary Concept]
- chromosome 6pter-P24 deletion syndrome [MeSH Supplementary Concept]
- cole carpenter syndrome [MeSH Supplementary Concept]
- craniosynostosis with ocular abnormalities and hallucal defects [MeSH Supplementary Concept]
- cryptophthalmos, unilateral or bilateral, isolated [MeSH Supplementary Concept]
- dwarfism stiff joint ocular abnormalities [MeSH Supplementary Concept]
- foveal hypoplasia and anterior segment dysgenesis [MeSH Supplementary Concept]
- fronto-facio-nasal dysplasia [MeSH Supplementary Concept]
- frontoocular syndrome [MeSH Supplementary Concept]
- iridogoniodysgenesis and skeletal anomalies [MeSH Supplementary Concept]
- iridogoniodysgenesis type1 [MeSH Supplementary Concept]
- iridogoniodysgenesis, dominant type [MeSH Supplementary Concept]
- jejunal atresia with microcephaly and ocular anomalies [MeSH Supplementary Concept]
- joubert syndrome 2 [MeSH Supplementary Concept]
- joubert syndrome 9 [MeSH Supplementary Concept]
- kapur toriello syndrome [MeSH Supplementary Concept]
- kaufman oculocerebrofacial syndrome [MeSH Supplementary Concept]
- macrophthalmia, colobomatous, with microcornea [MeSH Supplementary Concept]
- maxillofacial dysostosis [MeSH Supplementary Concept]
- mesangial sclerosis, diffuse renal, with ocular abnormalities [MeSH Supplementary Concept]
- microcornea, glaucoma, and absent frontal sinuses [MeSH Supplementary Concept]
- nephrotic syndrome ocular anomalies [MeSH Supplementary Concept]
- nephrotic syndrome, congenital, with or without ocular abnormalities [MeSH Supplementary Concept]
- oculoauricular syndrome [MeSH Supplementary Concept]
- oculoauriculofrontonasal syndrome [MeSH Supplementary Concept]
- oculocerebrocutaneous syndrome [MeSH Supplementary Concept]
- oculodentodigital dysplasia [MeSH Supplementary Concept]
- oculodentodigital dysplasia, autosomal recessive [MeSH Supplementary Concept]
- oculomaxillofacial dysostosis [MeSH Supplementary Concept]
- oculopalatocerebral syndrome [MeSH Supplementary Concept]
- oculopalatoskeletal syndrome [MeSH Supplementary Concept]
- oculorenocerebellar syndrome [MeSH Supplementary Concept]
- pena shokeir syndrome type 2 [MeSH Supplementary Concept]
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH Supplementary Concept]
- peters anomaly [MeSH Supplementary Concept]
- pierson syndrome [MeSH Supplementary Concept]
- popliteal pterygium syndrome [MeSH Supplementary Concept]
- popliteal pterygium syndrome, lethal type [MeSH Supplementary Concept]
- prepapillary vascular loops [MeSH Supplementary Concept]
- pupil, Egg-Shaped [MeSH Supplementary Concept]
- pupillary membrane, persistence of [MeSH Supplementary Concept]
- rieger syndrome 2 [MeSH Supplementary Concept]
- rozin hertz goodman syndrome [MeSH Supplementary Concept]
- torsion dystonia with onset in infancy [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- eye [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Eye Disorder [NCIt concept]
- Congenital anomalies of eye [ICD-9 code]
- Congenital anomaly of eye (disorder) [SNOMED CT concept]
- Congenital deformity of eye [MedDRA LLT]
- Congenital eye deformity NOS [MedDRA LLT]
- Congenital eye disorder [MedDRA Preferred Term]
- Congenital malformation of eye, unspecified [ICD-10 Sub-category]
- Congenital malformation of eye, unspecified [ICD-10 Sub-category (who)]
- EYE ABNORMALITY [WHO-ART Preferred Term]
- EYE MALFORMATION [WHO-ART Preferred Term]
- Eye abnormality [MedDRA LLT]
- Eye abnormality NOS [MedDRA LLT]
- Eye deformity congenital NOS [MedDRA LLT]
- Eye disorders congenital [MedDRA High Level Group Term]
- Eye malformation [MedDRA LLT]
- Unspecified anomaly of eye [ICD-9 code]
- Unspecified anomaly of eye, congenital [MedDRA LLT]
- congenital anomaly of eye, nos [SNOMED Notion]
- eye malformation [BNCI symptom]
- eye malformation [Disease (Nov.)]
Validated automatic mappings to NTBT
- ocular disease [Artificial nutrition thesaurus concept]

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