Hypothermia
Symptom Information:
Symptom ID: | HPO:0002045 | ||||||||||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of temperature regulation(HPO:0004370) Hypothermia(HPO:0002045) MedDRA: Investigations(MedDRA:10022891) Physical examination and organ system status topics(MedDRA:10071940) Physical examination procedures and organ system status(MedDRA:10071941) Hypothermia(HPO:0002045) Injury, poisoning and procedural complications(MedDRA:10022117) Injuries by physical agents(MedDRA:10022119) Conditions caused by cold(MedDRA:10010269) Hypothermia(HPO:0002045) |
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Database Frequency: | 27 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
2-methylbutyryl-CoA dehydrogenase deficiency | (Orphanet:79157) |
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
Alexander disease | (Orphanet:58) |
Argininosuccinic aciduria | (Orphanet:23) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Citrullinemia type I | (Orphanet:247525) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Endomyocardial fibroelastosis | (Orphanet:2022) |
Erythromelalgia | (Orphanet:1956) |
Familial advanced sleep-phase syndrome | (Orphanet:164736) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Menkes disease | (Orphanet:565) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Neonatal hemochromatosis | (Orphanet:446) |
Occipital horn syndrome | (Orphanet:198) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Primary congenital hypothyroidism | (Orphanet:226295) |
Spontaneous periodic hypothermia | (Orphanet:29822) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Timothy syndrome | (Orphanet:65283) |
Wolfram syndrome 1 | (OMIM:222300) |
Yellow fever | (Orphanet:99829) |