Weight loss
Symptom Information:
Symptom ID: | HPO:0001824 | |||||||||||||||||
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) Growth abnormality(HPO:0001507) Abnormality of body weight(HPO:0004323) Decreased body weight(HPO:0004325) Weight loss(HPO:0001824) MedDRA: Investigations(MedDRA:10022891) Physical examination and organ system status topics(MedDRA:10071940) Physical examination procedures and organ system status(MedDRA:10071941) Weight loss(HPO:0001824) |
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Database Frequency: | 42 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Adult heart tumor | (Orphanet:874) |
Autosomal recessive infantile hypercalcemia | (Orphanet:300547) |
Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
Carney complex | (Orphanet:1359) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Citrullinemia type I | (Orphanet:247525) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fatal familial insomnia | (Orphanet:466) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Huntington disease | (Orphanet:399) |
Huntington disease-like 2 | (Orphanet:98934) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
INFLAMMATORY BOWEL DISEASE 1 | (OMIM:266600) |
INFLAMMATORY BOWEL DISEASE 11 | (OMIM:191390) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
MELAS | (Orphanet:550) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy | (Orphanet:255235) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
Nephronophthisis 1 | (OMIM:256100) |
Neuroblastoma | (Orphanet:635) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT | (OMIM:605543) |
Pachygyria - epilepsy - intellectual deficit - dysmorphism | (Orphanet:94084) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pediatric systemic sclerosis | (Orphanet:93567) |
Perry syndrome | (Orphanet:178509) |
Primary systemic amyloidosis | (Orphanet:314701) |
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 | (OMIM:181000) |
Sarcoidosis | (Orphanet:797) |
Senile systemic amyloidosis | (Orphanet:330001) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |