Cutaneous photosensitivity
Symptom Information:
Symptom ID: | HPO:0000992 | |||||||||||||||||||||||||||||||||||||||||||||
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 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) |
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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) |