Retinopathy

Symptom Information:

Symptom ID: HPO:0000488
Synonyms:
Retinopathy (disorder) [Orphanet:5270]
Retinal disorder (disorder) [Orphanet:5270]
Retinal Diseases [Orphanet:5270]
Retinopathy [OMIM:Retinopathy]
Retinopathy [Orphanet:5270]
Retinal disorder [Orphanet:5270]
Retinal disorder [MedDRA:10038853]
Blister on macula of eye [MedDRA:10038853]
Disorder retinal [MedDRA:10038853]
Other retinal disorders [MedDRA:10038853]
Other specified retinal disorder [MedDRA:10038853]
Other specified retinal disorders [MedDRA:10038853]
Retinal blister [MedDRA:10038853]
Retinal defect, unspecified [MedDRA:10038853]
Retinal defects without detachment [MedDRA:10038853]
Retinal disorder NOS [MedDRA:10038853]
Retinal nerve fiber bundle defects [MedDRA:10038853]
Retinal opacity [MedDRA:10038853]
Unspecified retinal disorder [MedDRA:10038853]
Retinal fovea disorder [MedDRA:10038853]
Retinopathy [MedDRA:10038923]
Retinal arterial nipping [MedDRA:10038923]
Retinal AV nipping [MedDRA:10038923]
Retinopathy N0S [MedDRA:10038923]
Varying retinal vessel calibre [MedDRA:10038923]
Retinopathy NOS [MedDRA:10038923]
Retinal arteriovenous nicking [MedDRA:10038923]
No retinopathy [OMIM:No retinopathy]
Retinopathy (in some patients) [OMIM:Retinopathy (in some patients)]
Retinopathy (rare) [OMIM:Retinopathy (rare)]
Quality:
Cross references:
Orphanet:5270 "Retinopathy" [Orphanet:5270]
OMIM: "Retinopathy" [OMIM:Retinopathy]
OMIM: "No retinopathy" [OMIM:No retinopathy]
OMIM: "Retinopathy (in some patients)" [OMIM:Retinopathy (in some patients)]
OMIM: "Retinopathy (rare)" [OMIM:Retinopathy (rare)]
UMLS:C1962966 "Retinopathy" [HPO:0000488]
UMLS:C0035309 "Retinal Diseases" [Orphanet:5270]
Is a (Direct Parents):
MedDRA Retinopathies NEC
MedDRA Ocular disorders NEC
HPO         Abnormality of the retina
Orphanet Abnormality of the eye
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Retinopathy(HPO:0000488)
MedDRA:
Eye disorders(MedDRA:10015919)
    Eye disorders NEC(MedDRA:10015917)
       Ocular disorders NEC(MedDRA:10030032)
          Retinopathy(HPO:0000488)
    Retina, choroid and vitreous haemorrhages and vascular disorders(MedDRA:10047060)
       Retinopathies NEC(MedDRA:10038932)
          Retinopathy(HPO:0000488)
Database Frequency: 75 / 7739
Resource:

All diseases associated with this symptom:

Abetalipoproteinemia (Orphanet:14)
Aceruloplasminemia (Orphanet:48818)
Adult neuronal ceroid lipofuscinosis (Orphanet:79262)
Alport syndrome (Orphanet:63)
Alström syndrome (Orphanet:64)
Autosomal recessive Stickler syndrome (Orphanet:250984)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
Behçet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Bohring-Opitz syndrome (Orphanet:97297)
CHARGE syndrome (Orphanet:138)
CLN7 disease (Orphanet:228366)
CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE (OMIM:219900)
Cerebroretinal vasculopathy (Orphanet:3421)
Cockayne syndrome (Orphanet:191)
Cystinosis (Orphanet:213)
Cystinosis, adult nonnephropathic (OMIM:219750)
DPM1-CDG (Orphanet:79322)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
EEM syndrome (Orphanet:1897)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Familial melanoma (Orphanet:618)
Gaucher disease (Orphanet:355)
Granulomatosis with polyangiitis (Orphanet:900)
HERNS syndrome (Orphanet:63261)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hereditary vascular retinopathy (Orphanet:71291)
Holoprosencephaly (Orphanet:2162)
Hurler syndrome (Orphanet:93473)
Insulin-resistance syndrome type A (Orphanet:2297)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 20 (OMIM:614970)
Joubert syndrome 21 (OMIM:615636)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
Karsch-Neugebauer syndrome (Orphanet:2329)
Kniest dysplasia (Orphanet:485)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)
Linear verrucous nevus syndrome (Orphanet:2611)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2 (OMIM:616171)
Maternally-inherited diabetes and deafness (Orphanet:225)
Maturity-onset diabetes of the young, type 2 (OMIM:125851)
Maturity-onset diabetes of the young, type 3 (OMIM:600496)
Maturity-onset diabetes of the young, type 6 (OMIM:606394)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Mucolipidosis type 4 (Orphanet:578)
Mucopolysaccharidosis type 1 (Orphanet:579)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Neurodegeneration with brain iron accumulation (Orphanet:385)
Neutral lipid storage disease (Orphanet:165)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Pseudoxanthoma elasticum (Orphanet:758)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
Refsum disease (Orphanet:773)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Rift valley fever (Orphanet:319251)
Sea-blue histiocytosis (Orphanet:158029)
Sialidosis type 1 (Orphanet:812)
Sickle cell anemia (Orphanet:232)
Sjögren-Larsson syndrome (Orphanet:816)
Stickler syndrome type 2 (Orphanet:90654)
Takayasu arteritis (Orphanet:3287)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wolfram syndrome 1 (OMIM:222300)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)
Yunis-Varon syndrome (Orphanet:3472)