Lethargy
Symptom Information:
Symptom ID: | HPO:0001254 | ||||||||
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) Reduced consciousness/confusion(HPO:0004372) Lethargy(HPO:0001254) MedDRA: |
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Database Frequency: | 104 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
2-methylbutyryl-CoA dehydrogenase deficiency | (Orphanet:79157) |
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY | (OMIM:210200) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Autosomal recessive infantile hypercalcemia | (Orphanet:300547) |
Barth syndrome | (Orphanet:111) |
Biotinidase deficiency | (Orphanet:79241) |
CACH syndrome | (Orphanet:135) |
CADASIL | (Orphanet:136) |
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO | (OMIM:615751) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine uptake deficiency | (Orphanet:158) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Citrullinemia type I | (Orphanet:247525) |
Citrullinemia type II | (Orphanet:247585) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Classic maple syrup urine disease | (Orphanet:268145) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Congenital lipoid adrenal hyperplasia due to STAR deficency | (Orphanet:90790) |
Congenital or early infantile CACH syndrome | (Orphanet:157713) |
Cree leukoencephalopathy | (Orphanet:99854) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
Dihydropyrimidine dehydrogenase deficiency | (Orphanet:1675) |
Dihydropyrimidinuria | (Orphanet:38874) |
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD | (OMIM:130950) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Fatal multiple mitochondrial dysfunction syndrome | (Orphanet:289573) |
Fructose-1,6-bisphosphatase deficiency | (Orphanet:348) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gamma-aminobutyric acid transaminase deficiency | (Orphanet:2066) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycine encephalopathy | (Orphanet:407) |
HYPERLYSINURIA WITH HYPERAMMONEMIA | (OMIM:238750) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hereditary fructose intolerance | (Orphanet:469) |
Heritable pulmonary arterial hypertension | (Orphanet:275777) |
His bundle tachycardia | (Orphanet:3283) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Idiopathic copper-associated cirrhosis | (Orphanet:209919) |
Idiopathic pulmonary arterial hypertension | (Orphanet:275766) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Isovaleric acidemia | (Orphanet:33) |
Juvenile or adult CACH syndrome | (Orphanet:157719) |
Late infantile CACH syndrome | (Orphanet:157716) |
MEGDEL syndrome | (Orphanet:352328) |
MELAS | (Orphanet:550) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 | (OMIM:615838) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 | (OMIM:605711) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 | (OMIM:614299) |
MYXEDEMA | (OMIM:255900) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Methylcobalamin deficiency type cblDv1 | (Orphanet:308380) |
Methylcobalamin deficiency type cblE | (Orphanet:2169) |
Methylmalonic acidemia with homocystinuria | (Orphanet:26) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Methylmalonic acidemia with homocystinuria, type cblD | (Orphanet:79283) |
Methylmalonic acidemia with homocystinuria, type cblF | (Orphanet:79284) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Neonatal hemochromatosis | (Orphanet:446) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Ovarioleukodystrophy | (Orphanet:99853) |
Pearson syndrome | (Orphanet:699) |
Progressive demyelinating neuropathy with bilateral striatal necrosis | (Orphanet:217396) |
Propionic acidemia | (Orphanet:35) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
THYROID DYSHORMONOGENESIS 1 | (OMIM:274400) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Transcobalamin deficiency | (Orphanet:859) |
VISCERAL STEATOSIS, CONGENITAL | (OMIM:228100) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Vitamin B12-responsive methylmalonic acidemia, type cblDv2 | (Orphanet:308442) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |