Cutaneous photosensitivity

Symptom Information:

Symptom ID: HPO:0000992
Synonyms:
Photosensitive skin [HPO:0000992]
Photosensitive skin rashes [HPO:0000992]
Photosensitivity [HPO:0000992]
Skin photosensitivity [HPO:0000992]
Sun sensitivity [HPO:0000992]
Skin photosensitivity [Orphanet:23210]
Photosensitivity (finding) [Orphanet:23210]
Photosensitivity of skin [Orphanet:23210]
Dermatitis, Phototoxic [Orphanet:23210]
Cutaneous photosensitivity [OMIM:Cutaneous photosensitivity]
Photosensitive skin [OMIM:Photosensitive skin]
Photosensitive skin rashes [OMIM:Photosensitive skin rashes]
Photosensitivity [OMIM:Photosensitivity]
Skin photosensitivity [OMIM:Skin photosensitivity]
Sun sensitivity [OMIM:Sun sensitivity]
Sun sensitivity [Orphanet:23210]
Photosensitivity reaction [MedDRA:10034972]
Contact dermatitis and other eczema due to solar radiation [MedDRA:10034972]
Dermatitis of exposed site [MedDRA:10034972]
Dermatitis photosensitive [MedDRA:10034972]
Eruption of exposed site [MedDRA:10034972]
Exogenous photosensitive eruption [MedDRA:10034972]
Heliosensitive rash [MedDRA:10034972]
Photosensitive dermatitis [MedDRA:10034972]
Photosensitive rash [MedDRA:10034972]
Photosensitive reaction [MedDRA:10034972]
Photosensitivity [MedDRA:10034972]
Photosensitivity (NOS) [MedDRA:10034972]
Photosensitivity allergic reac [MedDRA:10034972]
Photosensitivity allergic react [MedDRA:10034972]
Photosensitivity allergic reaction [MedDRA:10034972]
Photosensitivity reaction NOS [MedDRA:10034972]
Photosensitivity toxic reaction [MedDRA:10034972]
Photosensitized [MedDRA:10034972]
Phototoxicity [MedDRA:10034972]
Pink macular rash on exposed areas [MedDRA:10034972]
Rash photosensitivity [MedDRA:10034972]
Reaction photosensitivity (NOS) [MedDRA:10034972]
Solar sensitiveness [MedDRA:10034972]
Sun sensitivity [MedDRA:10034972]
Photosensitivity reaction (NOS) [MedDRA:10034972]
Photocontact dermatitis [MedDRA:10034972]
Phytophotodermatitis [MedDRA:10034972]
Photosensitivity (harderoporphyria and HCP) [OMIM:Photosensitivity (harderoporphyria and HCP)]
Photosensitivity (in some patients) [OMIM:Photosensitivity (in some patients)]
Quality:
Cross references:
Orphanet:23210 "Skin photosensitivity" [Orphanet:23210]
OMIM: "Cutaneous photosensitivity" [OMIM:Cutaneous photosensitivity]
OMIM: "Photosensitive skin" [OMIM:Photosensitive skin]
OMIM: "Photosensitive skin rashes" [OMIM:Photosensitive skin rashes]
OMIM: "Photosensitivity" [OMIM:Photosensitivity]
OMIM: "Skin photosensitivity" [OMIM:Skin photosensitivity]
OMIM: "Sun sensitivity" [OMIM:Sun sensitivity]
OMIM: "Photosensitivity (harderoporphyria and HCP)" [OMIM:Photosensitivity (harderoporphyria and HCP)]
OMIM: "Photosensitivity (in some patients)" [OMIM:Photosensitivity (in some patients)]
UMLS:C0349506 "Photosensitivity" [HPO:0000992]
UMLS:C0349506 "Photosensitivity of skin" [Orphanet:23210]
UMLS:C0162830 "Dermatitis, Phototoxic" [Orphanet:23210]
Is a (Direct Parents):
MedDRA Photosensitivity and photodermatosis conditions
HPO         Generalized abnormality of skin
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Cutaneous photosensitivity(HPO:0000992)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Photosensitivity and photodermatosis conditions(MedDRA:10072982)
          Cutaneous photosensitivity(HPO:0000992)
Database Frequency: 75 / 7739
Resource:

All diseases associated with this symptom:

ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY (OMIM:174770)
ADULT syndrome (Orphanet:978)
ATAXIA-TELANGIECTASIA-LIKE DISORDER 2 (OMIM:615919)
Ataxia - photosensitivity - short stature (Orphanet:1184)
Bloom syndrome (Orphanet:125)
CEREBROOCULOFACIOSKELETAL SYNDROME 2 (OMIM:610756)
CHILBLAIN LUPUS 2 (OMIM:614415)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
COFS syndrome (Orphanet:1466)
COMPLEMENT COMPONENT 4A DEFICIENCY (OMIM:614380)
Chronic granulomatous disease (Orphanet:379)
Cockayne syndrome (Orphanet:191)
Congenital erythropoietic porphyria (Orphanet:79277)
Cutaneous lupus erythematosus (Orphanet:535)
Cutaneous photosensitivity - lethal colitis (Orphanet:2881)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
Dermatomyositis (Orphanet:221)
Disseminated superficial actinic porokeratosis (Orphanet:79152)
Dubowitz syndrome (Orphanet:235)
Dyschromatosis universalis (Orphanet:241)
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3 (OMIM:608762)
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET (OMIM:615369)
Erythrokeratodermia variabilis (Orphanet:317)
Erythropoietic protoporphyria (Orphanet:79278)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hartnup syndrome (Orphanet:2116)
Hepatoerythropoietic porphyria (Orphanet:95159)
Hereditary acrokeratotic poikiloderma of Kindler-Weary (Orphanet:306539)
Hereditary coproporphyria (Orphanet:79273)
Hyperkeratosis-hyperpigmentation syndrome (Orphanet:1336)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Jessner's lymphocytic infiltration of the skin (Orphanet:33314)
Juvenile dermatomyositis (Orphanet:93672)
Kindler syndrome (Orphanet:2908)
LIG4 syndrome (Orphanet:99812)
Lafora disease (Orphanet:501)
Nijmegen breakage syndrome (Orphanet:647)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 3 (Orphanet:79433)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX (OMIM:260480)
PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED (OMIM:300752)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Piebald trait - neurologic defects (Orphanet:2885)
Porokeratosis (Orphanet:79358)
Porokeratosis of Mibelli (Orphanet:735)
Porphyria (Orphanet:738)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Porphyria variegata (Orphanet:79473)
Prader-Willi syndrome (Orphanet:739)
Prolidase deficiency (Orphanet:742)
Rothmund-Thomson syndrome (Orphanet:2909)
SYSTEMIC LUPUS ERYTHEMATOSUS (OMIM:152700)
Singleton-Merten dysplasia (Orphanet:85191)
Smith-Lemli-Opitz syndrome (Orphanet:818)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)
TRYPTOPHANURIA WITH DWARFISM (OMIM:276100)
UV-SENSITIVE SYNDROME 1 (OMIM:600630)
UV-SENSITIVE SYNDROME 2 (OMIM:614621)
UV-SENSITIVE SYNDROME 3 (OMIM:614640)
UV-sensitive syndrome (Orphanet:178338)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum complementation group A (Orphanet:276249)
Xeroderma pigmentosum complementation group B (Orphanet:276252)
Xeroderma pigmentosum complementation group C (Orphanet:276255)
Xeroderma pigmentosum complementation group D (Orphanet:276258)
Xeroderma pigmentosum complementation group E (Orphanet:276261)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Xeroderma pigmentosum complementation group G (Orphanet:276267)
Xeroderma pigmentosum variant (Orphanet:90342)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)