Pruritus

Symptom Information:

Symptom ID: HPO:0000989
Synonyms:
Itching of skin [HPO:0000989]
Itching (finding) [Orphanet:23380]
Pruritic disorders (disorder) [Orphanet:23380]
Itching of skin (finding) [Orphanet:23380]
Itch of skin (observable entity) [Orphanet:23380]
Pruritus [Orphanet:23380]
Pruritus [OMIM:Pruritus]
Pruritus/itching [Orphanet:23380]
Pruritus [MedDRA:10037087]
Extremities itchy sensation of [MedDRA:10037087]
Itch [MedDRA:10037087]
Itch burning [MedDRA:10037087]
Itching [MedDRA:10037087]
Itching both hands [MedDRA:10037087]
Itchy [MedDRA:10037087]
Itchy legs [MedDRA:10037087]
Itchy scalp [MedDRA:10037087]
Itchy skin [MedDRA:10037087]
Other specified pruritic conditions [MedDRA:10037087]
Pruritis [MedDRA:10037087]
Pruritus and related conditions [MedDRA:10037087]
Pruritus cutaneous [MedDRA:10037087]
Pruritus facial [MedDRA:10037087]
Pruritus NOS [MedDRA:10037087]
Pruritus of both hands [MedDRA:10037087]
Unspecified pruritic disorder [MedDRA:10037087]
Pruritus aggravated [MedDRA:10037087]
Pruritus breast [MedDRA:10037087]
Hairy skin itching [MedDRA:10037087]
Localised itching [MedDRA:10037087]
Localized itching [MedDRA:10037087]
Itch (in some patients) [OMIM:Itch (in some patients)]
Itching [OMIM:Itching]
Itching ( in some patients) [OMIM:Itching ( in some patients)]
Pruritis [OMIM:Pruritis]
Pruritus (inflammatory type B) [OMIM:Pruritus (inflammatory type B)]
Pruritus (major feature) [OMIM:Pruritus (major feature)]
Quality:
Cross references:
Orphanet:23380 "Pruritus/itching" [Orphanet:23380]
OMIM: "Pruritus" [OMIM:Pruritus]
OMIM: "Itch (in some patients)" [OMIM:Itch (in some patients)]
OMIM: "Itching" [OMIM:Itching]
OMIM: "Itching ( in some patients)" [OMIM:Itching ( in some patients)]
OMIM: "Pruritis" [OMIM:Pruritis]
OMIM: "Pruritus (inflammatory type B)" [OMIM:Pruritus (inflammatory type B)]
OMIM: "Pruritus (major feature)" [OMIM:Pruritus (major feature)]
UMLS:C0033774 "Pruritus" [HPO:0000989]
UMLS:C0033774 "Pruritus" [Orphanet:23380]
Is a (Direct Parents):
MedDRA Pruritus NEC
Orphanet Abnormality of the skin
HPO         Abnormality of skin physiology
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)
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)