Cachexia
Symptom Information:
Symptom ID: | HPO:0004326 | |||||||||||||
Synonyms: |
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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) 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) |
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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) |