Retinopathy
Symptom Information:
Symptom ID: | HPO:0000488 | ||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Retina, choroid and vitreous haemorrhages and vascular disorders(MedDRA:10047060) Retinopathies NEC(MedDRA:10038932) Retinopathy(HPO:0000488) Eye disorders NEC(MedDRA:10015917) Ocular disorders NEC(MedDRA:10030032) Retinopathy(HPO:0000488) |
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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) |