Cachexia

Symptom Information:

Symptom ID: HPO:0004326
Synonyms:
Cachexia (finding) [Orphanet:53050]
Cachexia [Orphanet:53050]
Wasting [Orphanet:53050]
Cachexia [OMIM:Cachexia]
Wasted (excluding lipodystrophy)/poorly muscled build/cachexy [Orphanet:53050]
Cachexia [MedDRA:10006895]
Emaciation [MedDRA:10006895]
Wasting [MedDRA:10006895]
Wasting generalized [MedDRA:10006895]
Cardiac cachexia [MedDRA:10006895]
Cancer cachexia [MedDRA:10006895]
Constitutional syndrome [MedDRA:10006895]
Wasting generalised [MedDRA:10006895]
Quality:
Cross references:
Orphanet:53050 "Wasted (excluding lipodystrophy)/poorly muscled build/cachexy" [Orphanet:53050]
OMIM: "Cachexia" [OMIM:Cachexia]
UMLS:C0006625 "Cachexia" [HPO:0004326]
UMLS:C0006625 "Cachexia" [Orphanet:53050]
UMLS:C0235394 "Wasting" [Orphanet:53050]
Is a (Direct Parents):
MedDRA Asthenic conditions
Orphanet Build/stature/longevity anomalies
HPO         Weight loss
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)
                   Cachexia(HPO:0004326)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       Asthenic conditions(MedDRA:10003550)
          Cachexia(HPO:0004326)
Database Frequency: 71 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
AREDYLD syndrome (Orphanet:1133)
Arachnodactyly - intellectual deficit - dysmorphism (Orphanet:1130)
Arthrogryposis-like hand anomaly - sensorineural deafness (Orphanet:1144)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Autosomal dominant congenital benign spinal muscular atrophy (Orphanet:1216)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Bethlem myopathy (Orphanet:610)
Cabezas syndrome (Orphanet:85293)
Choroideremia - hypopituitarism (Orphanet:1434)
Christianson syndrome (Orphanet:85278)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Cronkhite-Canada syndrome (Orphanet:2930)
Cutaneous photosensitivity - lethal colitis (Orphanet:2881)
Cutis laxa (Orphanet:209)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Desmoplastic small round cell tumor (Orphanet:83469)
Diencephalic syndrome (Orphanet:1672)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Eosinophilic granuloma (Orphanet:99871)
FACES syndrome (Orphanet:1969)
Flynn-Aird syndrome (Orphanet:2047)
Fried syndrome (Orphanet:85335)
Friedreich ataxia 1 (OMIM:229300)
Fryns-Smeets-Thiry syndrome (Orphanet:2058)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior (Orphanet:85329)
Intellectual deficit, X-linked, Miles-Carpenter type (Orphanet:85283)
Leprechaunism (Orphanet:508)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
MELAS (Orphanet:550)
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
Majeed syndrome (Orphanet:77297)
Marfan syndrome (Orphanet:558)
McDonough syndrome (Orphanet:2471)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy (Orphanet:255235)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Moynahan syndrome (Orphanet:2574)
Mulibrey nanism (Orphanet:2576)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multicentric reticulohistiocytosis (Orphanet:139436)
Nijmegen breakage syndrome (Orphanet:647)
Norrie disease (Orphanet:649)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Pelizaeus-Merzbacher disease (Orphanet:702)
Progressive nodular histiocytosis (Orphanet:158022)
Proteus syndrome (Orphanet:744)
Renpenning syndrome (Orphanet:3242)
Rett syndrome (Orphanet:778)
Riboflavin transporter deficiency (Orphanet:97229)
Ring chromosome 10 (Orphanet:1438)
Schwartz-Jampel syndrome (Orphanet:800)
Scleroderma (Orphanet:801)
Seckel syndrome (Orphanet:808)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Silver-Russell syndrome (Orphanet:813)
Stickler syndrome (Orphanet:828)
Systemic sclerosis (Orphanet:90291)
Tetrasomy 12p (Orphanet:884)
Trisomy 18 (Orphanet:3380)
Whipple disease (Orphanet:3452)
Wolman disease (Orphanet:75233)
X-linked creatine transporter deficiency (Orphanet:52503)
XFE PROGEROID SYNDROME (OMIM:610965)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)