Pruritus
Symptom Information:
Symptom ID: | HPO:0000989 | |||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||
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) Abnormality of skin physiology(HPO:0011122) Pruritus(HPO:0000989) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Pruritus NEC(MedDRA:10049293) Pruritus(HPO:0000989) |
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Database Frequency: | 111 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1 | (OMIM:105250) |
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2 | (OMIM:613955) |
ARTHRITIS, SACROILIAC | (OMIM:108100) |
Acquired epidermolysis bullosa | (Orphanet:46487) |
Acquired ichthyosis | (Orphanet:454) |
Adult Still's disease | (Orphanet:829) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alveolar echinococcosis | (Orphanet:284) |
Antisynthetase syndrome | (Orphanet:81) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Benign recurrent intrahepatic cholestasis type 2 | (Orphanet:99961) |
Bullous diffuse cutaneous mastocytosis | (Orphanet:280785) |
Bullous lichen planus | (Orphanet:33408) |
CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE | (OMIM:214980) |
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3 | (OMIM:614972) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cholangiocarcinoma | (Orphanet:70567) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Classical mycosis fungoides | (Orphanet:2584) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Congenital non-bullous ichthyosiform erythroderma | (Orphanet:79394) |
Cutaneous lupus erythematosus | (Orphanet:535) |
Cutaneous mastocytoma | (Orphanet:79455) |
Cutaneous mastocytosis | (Orphanet:66646) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Darier disease | (Orphanet:218) |
Dengue fever | (Orphanet:99828) |
Dermatitis herpetiformis | (Orphanet:1656) |
Dermatomyositis | (Orphanet:221) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Dissecting cellulitis of the scalp | (Orphanet:345) |
Disseminated superficial actinic porokeratosis | (Orphanet:79152) |
Dracunculiasis | (Orphanet:231) |
Dystrophic epidermolysis bullosa pruriginosa | (Orphanet:89843) |
EPISODIC PAIN SYNDROME, FAMILIAL, 2 | (OMIM:615551) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Erythromelalgia | (Orphanet:1956) |
Erythropoietic protoporphyria | (Orphanet:79278) |
Familial cold urticaria | (Orphanet:47045) |
Familial hypercholanemia | (Orphanet:238475) |
Familial leiomyomatosis | (Orphanet:523) |
Familial primary localized cutaneous amyloidosis | (Orphanet:353220) |
Familial thrombocytosis | (Orphanet:71493) |
Generalized peeling skin syndrome | (Orphanet:263543) |
Graham Little-Piccardi-Lassueur syndrome | (Orphanet:505) |
HYPOTRICHOSIS 6 | (OMIM:607903) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hydatidosis | (Orphanet:400) |
Hyperkeratosis lenticularis perstans | (Orphanet:409) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypotrichosis simplex | (Orphanet:55654) |
ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT | (OMIM:146750) |
Idiopathic hypereosinophilic syndrome | (Orphanet:3260) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Inherited epidermolysis bullosa | (Orphanet:79361) |
Intrahepatic cholestasis of pregnancy | (Orphanet:69665) |
Jessner's lymphocytic infiltration of the skin | (Orphanet:33314) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Juvenile dermatomyositis | (Orphanet:93672) |
Keratosis pilaris atrophicans | (Orphanet:498) |
Lamellar ichthyosis | (Orphanet:313) |
Large congenital melanocytic nevus | (Orphanet:626) |
Lichen amyloidosis | (Orphanet:49804) |
Lichen planopilaris | (Orphanet:525) |
Linear IgA dermatosis | (Orphanet:46488) |
MELAS | (Orphanet:550) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
Malakoplakia | (Orphanet:556) |
Mastocytosis | (Orphanet:98292) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Nephronophthisis 1 | (OMIM:256100) |
Nodular lymphocyte predominant Hodgkin lymphoma | (Orphanet:86893) |
Non-epidermolytic palmoplantar keratoderma | (Orphanet:2337) |
Non-histaminic angioedema | (Orphanet:658) |
Omenn syndrome | (Orphanet:39041) |
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX | (OMIM:260480) |
PROTOPORPHYRIA, ERYTHROPOIETIC | (OMIM:177000) |
PRURITUS, HEREDITARY LOCALIZED | (OMIM:177100) |
Peeling skin syndrome type B | (Orphanet:263553) |
Pemphigus erythematosus | (Orphanet:79480) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Porokeratosis | (Orphanet:79358) |
Porokeratosis of Mibelli | (Orphanet:735) |
Porphyria | (Orphanet:738) |
Pretibial dystrophic epidermolysis bullosa | (Orphanet:79410) |
Primary cutaneous anaplastic large cell lymphoma | (Orphanet:300865) |
Primary cutaneous lymphoma | (Orphanet:542) |
Primary familial polycythemia | (Orphanet:90042) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Progressive familial intrahepatic cholestasis type 1 | (Orphanet:79306) |
Progressive familial intrahepatic cholestasis type 2 | (Orphanet:79304) |
Progressive familial intrahepatic cholestasis type 3 | (Orphanet:79305) |
Prolidase deficiency | (Orphanet:742) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Reynolds syndrome | (Orphanet:779) |
Schnitzler syndrome | (Orphanet:37748) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Subcorneal pustular dermatosis | (Orphanet:48377) |
Sézary syndrome | (Orphanet:3162) |
Wells syndrome | (Orphanet:901) |