Hypothermia

Symptom Information:

Symptom ID: HPO:0002045
Synonyms:
Hypothermia (finding) [Orphanet:54560]
Hypothermia, natural [Orphanet:54560]
Hypothermia [OMIM:Hypothermia]
Hypothermia [Orphanet:54560]
Body temperature decreased [Orphanet:54560]
Body temperature decreased [MedDRA:10005910]
Body temperature decrease [MedDRA:10005910]
Temperature body decrease [MedDRA:10005910]
Hypothermia [MedDRA:10021113]
Hypopyrexia [MedDRA:10021113]
Quality:
Cross references:
Orphanet:54560 "Hypothermia" [Orphanet:54560]
OMIM: "Hypothermia" [OMIM:Hypothermia]
UMLS:C2364050 "Hypothermia" [HPO:0002045]
UMLS:C0020672 "Hypothermia, natural" [Orphanet:54560]
Is a (Direct Parents):
MedDRA Physical examination procedures and organ system status
MedDRA Conditions caused by cold
Orphanet Health status anomalies
HPO         Abnormality of temperature regulation
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)
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)