Anorexia
Symptom Information:
Symptom ID: | HPO:0002039 | ||||||||||||||||||||||||||||||||||
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 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) |
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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) |