Weight loss

Symptom Information:

Symptom ID: HPO:0001824
Synonyms:
Weight decreasing (finding) [Orphanet:54070]
Weight loss finding (finding) [Orphanet:54070]
Weight decreased (finding) [Orphanet:54070]
Body Weight decreased [Orphanet:54070]
Weight loss [OMIM:Weight loss]
Weight loss/loss of appetite/break in weight curve/general health alteration [Orphanet:54070]
Weight decreased [Orphanet:54070]
Weight decreased [MedDRA:10047895]
Losing wt [MedDRA:10047895]
Loss of weight [MedDRA:10047895]
Lost weight [MedDRA:10047895]
Weight decrease [MedDRA:10047895]
Weight loss [MedDRA:10047895]
Wt loss [MedDRA:10047895]
Weight below normal [MedDRA:10047895]
Weight loss (with disseminated disease) [OMIM:Weight loss (with disseminated disease)]
General health alteration [Orphanet:54070]
Quality:
Cross references:
Orphanet:54070 "Weight loss/loss of appetite/break in weight curve/general health alteration" [Orphanet:54070]
OMIM: "Weight loss" [OMIM:Weight loss]
OMIM: "Weight loss (with disseminated disease)" [OMIM:Weight loss (with disseminated disease)]
UMLS:C0043096 "Body Weight decreased" [Orphanet:54070]
Is a (Direct Parents):
Orphanet Failure to thrive
MedDRA Physical examination procedures and organ system status
HPO         Decreased body weight
Orphanet Health status anomalies
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)
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)