Fatigue

Symptom Information:

Symptom ID: HPO:0012378
Synonyms:
Fatigue (1 patient) [OMIM:Fatigue (1 patient)]
Quality:
Cross references:
OMIM: "Fatigue (1 patient)" [OMIM:Fatigue (1 patient)]
Is a (Direct Parents):
HPO         Behavioral abnormality
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:
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)