Fatigue
Symptom Information:
Symptom ID: | HPO:0012378 | ||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Fatigue(HPO:0012378) MedDRA: |
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Database Frequency: | 50 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ANALBUMINEMIA | (OMIM:616000) |
Acute interstitial pneumonia | (Orphanet:79126) |
Adiposis dolorosa | (Orphanet:36397) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Barth syndrome | (Orphanet:111) |
Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
CREST syndrome | (Orphanet:90290) |
Chuvash erythrocytosis | (Orphanet:238557) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Fabry disease | (Orphanet:324) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial isolated restrictive cardiomyopathy | (Orphanet:75249) |
Familial sick sinus syndrome | (Orphanet:166282) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
GLUCOCORTICOID RESISTANCE, GENERALIZED | (OMIM:615962) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY | (OMIM:241150) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 2A | (OMIM:602390) |
Heritable pulmonary arterial hypertension | (Orphanet:275777) |
Hypouricemia, renal, 2 | (OMIM:612076) |
Idiopathic pulmonary arterial hypertension | (Orphanet:275766) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
MERRF | (Orphanet:551) |
MYXEDEMA | (OMIM:255900) |
Myopathy due to myoadenylate deaminase deficiency | (OMIM:615511) |
Naxos disease | (Orphanet:34217) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | (OMIM:615399) |
PGM1-CDG | (Orphanet:319646) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Peripartum cardiomyopathy | (Orphanet:563) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary familial polycythemia | (Orphanet:90042) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Wolfram syndrome 1 | (OMIM:222300) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |