Anorexia

Symptom Information:

Symptom ID: HPO:0002039
Synonyms:
Anorexia nervosa [Orphanet:43600]
Anorexia nervosa (disorder) [Orphanet:43600]
Anorexia symptom (finding) [Orphanet:54070]
Anorexic [Orphanet:54070]
anorexia [HPO:0002039]
Anorexia Nervosa [Orphanet:43600]
Loss of appetite (finding) [Orphanet:54070]
Anorexia symptom [Orphanet:54070]
Anorexia [Orphanet:54070]
Anorexia [OMIM:Anorexia]
Anorexia [Orphanet:43600]
Weight loss/loss of appetite/break in weight curve/general health alteration [Orphanet:54070]
Appetite lost [Orphanet:54070]
Anorectic [Orphanet:54070]
Inappetence [Orphanet:54070]
Anorexia nervosa [MedDRA:10002649]
Slimmers disease [MedDRA:10002649]
Decreased appetite [MedDRA:10061428]
Anorexia [MedDRA:10061428]
Anorexic [MedDRA:10061428]
Appetite absent [MedDRA:10061428]
Appetite decreased NOS [MedDRA:10061428]
Appetite impaired [MedDRA:10061428]
Appetite lost [MedDRA:10061428]
Appetite suppressed [MedDRA:10061428]
Appetite suppression [MedDRA:10061428]
Anorectic [MedDRA:10061428]
Inappetence [MedDRA:10061428]
Anorexia post chemotherapy [MedDRA:10061428]
Hyporexia [MedDRA:10061428]
Decreased appetite [OMIM:Decreased appetite]
Loss of appetite [OMIM:Loss of appetite]
Loss of appetite (in some patients) [OMIM:Loss of appetite (in some patients)]
General health alteration [Orphanet:54070]
Quality:
Cross references:
Orphanet:43600 "Anorexia" [Orphanet:43600]
Orphanet:54070 "Weight loss/loss of appetite/break in weight curve/general health alteration" [Orphanet:54070]
OMIM: "Anorexia" [OMIM:Anorexia]
OMIM: "Decreased appetite" [OMIM:Decreased appetite]
OMIM: "Loss of appetite" [OMIM:Loss of appetite]
OMIM: "Loss of appetite (in some patients)" [OMIM:Loss of appetite (in some patients)]
UMLS:C0426579 "anorexia" [HPO:0002039]
UMLS:C0003125 "Anorexia Nervosa" [Orphanet:43600]
UMLS:C1971624 "Loss of appetite (finding)" [Orphanet:54070]
UMLS:C0426579 "Anorexia symptom" [Orphanet:54070]
UMLS:C0003123 "Anorexia" [Orphanet:54070]
Is a (Direct Parents):
HPO         Abdominal symptom
Orphanet Behavioral abnormality
MedDRA Appetite disorders
Orphanet Failure to thrive
Orphanet Health status anomalies
MedDRA Eating disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abdominal symptom(HPO:0011458)
             Anorexia(HPO:0002039)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Appetite and general nutritional disorders(MedDRA:10003018)
       Appetite disorders(MedDRA:10003022)
          Anorexia(HPO:0002039)
Database Frequency: 62 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acute intermittent porphyria (Orphanet:79276)
Aggressive systemic mastocytosis (Orphanet:98850)
Argininemia (Orphanet:90)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Babesiosis (Orphanet:108)
Behçet disease (Orphanet:117)
Benign recurrent intrahepatic cholestasis (Orphanet:65682)
Blue diaper syndrome (Orphanet:94086)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Camurati-Engelmann disease (Orphanet:1328)
Carcinoma of the gallbladder (Orphanet:56044)
Carney triad (Orphanet:139411)
Cholangiocarcinoma (Orphanet:70567)
Classical homocystinuria (Orphanet:394)
Cronkhite-Canada syndrome (Orphanet:2930)
Cystinosis (Orphanet:213)
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY (OMIM:600351)
Fabry disease (Orphanet:324)
Gaucher disease type 2 (Orphanet:77260)
Giant cell arteritis (Orphanet:397)
Hereditary folate malabsorption (Orphanet:90045)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hypernychthemeral syndrome (Orphanet:73267)
Immunoglobulin A vasculitis (Orphanet:761)
Infant botulism (Orphanet:178478)
Infantile hypophosphatasia (Orphanet:247651)
Legionellosis (Orphanet:549)
Leigh syndrome (Orphanet:506)
MELAS (Orphanet:550)
Mantle cell lymphoma (Orphanet:52416)
Mastocytosis (Orphanet:98292)
Menetrier disease (Orphanet:2494)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblD (Orphanet:79283)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Nipah virus disease (Orphanet:99825)
Nodular lymphocyte predominant Hodgkin lymphoma (Orphanet:86893)
Ornithine transcarbamylase deficiency (Orphanet:664)
Pearson syndrome (Orphanet:699)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Polymyositis (Orphanet:732)
Porphyria (Orphanet:738)
Primary systemic amyloidosis (Orphanet:314701)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Propionic acidemia (Orphanet:35)
Proximal renal tubular acidosis (Orphanet:47159)
Rabies (Orphanet:770)
Rheumatic fever (Orphanet:3099)
Rift valley fever (Orphanet:319251)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
Sarcoidosis (Orphanet:797)
TERATOMA, PINEAL (OMIM:273120)
Takayasu arteritis (Orphanet:3287)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
Yellow fever (Orphanet:99829)