Photophobia

Symptom Information:

Symptom ID: HPO:0000613
Synonyms:
Photodysphoria [HPO:0000613]
Eyes sensitive to light (finding) [Orphanet:5720]
Photophobia (finding) [Orphanet:5720]
Photophobia [Orphanet:5720]
Photophobia [OMIM:Photophobia]
Photophobia [MedDRA:10034960]
Exacerbation of photophobia [MedDRA:10034960]
Eyes sensitive to sunlight [MedDRA:10034960]
Photophobia aggravated [MedDRA:10034960]
Light sensitivity to eye [MedDRA:10034960]
Photophobia (early symptom) [OMIM:Photophobia (early symptom)]
Photophobia (in some patients) [OMIM:Photophobia (in some patients)]
Photophobia (infancy) [OMIM:Photophobia (infancy)]
Photophobia (rare) [OMIM:Photophobia (rare)]
Quality:
Cross references:
Orphanet:5720 "Photophobia" [Orphanet:5720]
OMIM: "Photophobia" [OMIM:Photophobia]
OMIM: "Photophobia (early symptom)" [OMIM:Photophobia (early symptom)]
OMIM: "Photophobia (in some patients)" [OMIM:Photophobia (in some patients)]
OMIM: "Photophobia (infancy)" [OMIM:Photophobia (infancy)]
OMIM: "Photophobia (rare)" [OMIM:Photophobia (rare)]
UMLS:C0085636 "Photophobia" [HPO:0000613]
UMLS:C0085636 "Photophobia" [Orphanet:5720]
Is a (Direct Parents):
HPO         Abnormality of vision
Orphanet Abnormality of the eye
HPO         Behavioral abnormality
MedDRA Ocular signs and symptoms NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Behavioral abnormality(HPO:0000708)
                   Photophobia(HPO:0000613)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of vision(HPO:0000504)
                Photophobia(HPO:0000613)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders of the eye(MedDRA:10029301)
       Ocular signs and symptoms NEC(MedDRA:10030952)
          Photophobia(HPO:0000613)
Database Frequency: 158 / 7739
Resource:

All diseases associated with this symptom:

ACHROMATOPSIA 2 (OMIM:216900)
ACHROMATOPSIA 3 (OMIM:262300)
ACHROMATOPSIA 4 (OMIM:613856)
ALACRIMA, CONGENITAL (OMIM:103420)
ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE (OMIM:601549)
ATAXIA-TELANGIECTASIA-LIKE DISORDER 2 (OMIM:615919)
Achromatopsia (Orphanet:49382)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Alport syndrome (Orphanet:63)
Alström syndrome (Orphanet:64)
Amaurosis - hypertrichosis (Orphanet:1021)
Aniridia (Orphanet:77)
Arnold-Chiari malformation type I (Orphanet:268882)
Ataxia - hypogonadism - choroidal dystrophy (Orphanet:1180)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autosomal recessive optic atrophy, OPA6 type (Orphanet:99012)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BRESEK syndrome (Orphanet:85284)
Babesiosis (Orphanet:108)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 5 (OMIM:615983)
Behçet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Blue cone monochromatism (Orphanet:16)
Bradyopsia (Orphanet:75374)
Butterfly-shaped pigment dystrophy (Orphanet:99001)
CATARACT 2, MULTIPLE TYPES (OMIM:604307)
CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2 (OMIM:613105)
CONE DYSTROPHY 3 (OMIM:602093)
CONE DYSTROPHY 4 (OMIM:613093)
CONE-ROD DYSTROPHY 10 (OMIM:610283)
CONE-ROD DYSTROPHY 11 (OMIM:610381)
CONE-ROD DYSTROPHY 13 (OMIM:608194)
CONE-ROD DYSTROPHY 15 (OMIM:613660)
CONE-ROD DYSTROPHY 17 (OMIM:615163)
CONE-ROD DYSTROPHY 5 (OMIM:600977)
CONE-ROD DYSTROPHY 8 (OMIM:605549)
CONE-ROD DYSTROPHY, X-LINKED, 1 (OMIM:304020)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Chédiak-Higashi syndrome (Orphanet:167)
Classical progressive supranuclear palsy (Orphanet:240071)
Cogan syndrome (Orphanet:1467)
Cone dystrophy with supernormal rod response (Orphanet:209932)
Cone rod dystrophy (Orphanet:1872)
Cystinosis (Orphanet:213)
Cystinosis, adult nonnephropathic (OMIM:219750)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ermine phenotype (Orphanet:999)
FLOTCH syndrome (Orphanet:2045)
Familial LCAT deficiency (Orphanet:79293)
Fleck corneal dystrophy (Orphanet:98970)
GLAUCOMA 3, PRIMARY CONGENITAL, D (OMIM:613086)
Gelatinous drop-like corneal dystrophy (Orphanet:98957)
Hartnup syndrome (Orphanet:2116)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary benign intraepithelial dyskeratosis (Orphanet:352657)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hidrotic ectodermal dysplasia (Orphanet:189)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Isolated congenital alacrima (Orphanet:91416)
Jalili syndrome (Orphanet:1873)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
KID syndrome (Orphanet:477)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
LCAT deficiency (Orphanet:650)
Leber congenital amaurosis 1 (OMIM:204000)
Leber congenital amaurosis 14 (OMIM:613341)
Leber congenital amaurosis 2 (OMIM:204100)
Leber congenital amaurosis 6 (OMIM:613826)
Leber congenital amaurosis 7 (OMIM:613829)
Leber congenital amaurosis 9 (OMIM:608553)
Leukonychia totalis (Orphanet:2387)
Lyell syndrome (Orphanet:537)
Lyme disease (Orphanet:91546)
Lymphedema - distichiasis (Orphanet:33001)
MELAS (Orphanet:550)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 (OMIM:157300)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10 (OMIM:610208)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11 (OMIM:610209)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3 (OMIM:607498)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5 (OMIM:607508)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6 (OMIM:607516)
MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4 (OMIM:607501)
MIGRAINE, FAMILIAL HEMIPLEGIC, 3 (OMIM:609634)
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 (OMIM:300125)
Macular corneal dystrophy (Orphanet:98969)
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen (Orphanet:251279)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Mucolipidosis type 4 (Orphanet:578)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (OMIM:610427)
Ocular albinism (Orphanet:284804)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)
Ocular albinism with late-onset sensorineural deafness (Orphanet:1000)
Oculocerebral hypopigmentation syndrome, Preus type (Orphanet:2720)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1 (Orphanet:352731)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 1B (Orphanet:79434)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 4 (Orphanet:79435)
Oculocutaneous albinism type 5 (Orphanet:370091)
Oculocutaneous albinism type 6 (Orphanet:370097)
Oculocutaneous albinism type 7 (Orphanet:352745)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Oligocone trichromacy (Orphanet:75378)
Progressive cone dystrophy (Orphanet:1871)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
RED SKIN PIGMENT ANOMALY OF NEW GUINEA (OMIM:266350)
RETINAL CONE DYSTROPHY 1 (OMIM:180020)
RETINAL CONE DYSTROPHY 3A (OMIM:610024)
RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELLABNORMALITIES (OMIM:616079)
RETINITIS PIGMENTOSA 37 (OMIM:611131)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
Reactive arthritis (Orphanet:29207)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Reis-Bücklers corneal dystrophy (Orphanet:98961)
Retinitis pigmentosa (Orphanet:791)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Rift valley fever (Orphanet:319251)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Sarcoidosis (Orphanet:797)
Scrub typhus (Orphanet:83317)
Short tarsus - absence of lower eyelashes (Orphanet:2832)
Sjögren-Larsson syndrome (Orphanet:816)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Stevens-Johnson syndrome (Orphanet:36426)
Temperature-sensitive oculocutaneous albinism type 1 (Orphanet:352737)
Thiel-Behnke corneal dystrophy (Orphanet:98960)
Tyrosinemia type 2 (Orphanet:28378)
USHER SYNDROME, TYPE IIIB (OMIM:614504)
X-linked recessive ocular albinism (Orphanet:54)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum complementation group A (Orphanet:276249)
Xeroderma pigmentosum complementation group C (Orphanet:276255)
Xeroderma pigmentosum complementation group D (Orphanet:276258)
Xeroderma pigmentosum complementation group E (Orphanet:276261)
Xeroderma pigmentosum variant (Orphanet:90342)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)
Yellow fever (Orphanet:99829)