Heat intolerance

Symptom Information:

Symptom ID: HPO:0002046
Synonyms:
Intolerance to heat and fevers [HPO:0002046]
Intolerant of heat [HPO:0002046]
Intolerant of heat (finding) [Orphanet:23020]
Intolerant of heat [Orphanet:23020]
Intolerance to heat and fevers [OMIM:Intolerance to heat and fevers]
Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance [Orphanet:23020]
Heat sensitivity [Orphanet:23020]
Temperature intolerance [MedDRA:10057040]
Cold intolerance [MedDRA:10057040]
Heat intolerance [MedDRA:10057040]
Heat sensitivity [MedDRA:10057040]
Intolerance to heat and fever [OMIM:Intolerance to heat and fever]
Quality:
Cross references:
Orphanet:23020 "Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance" [Orphanet:23020]
OMIM: "Intolerance to heat and fevers" [OMIM:Intolerance to heat and fevers]
OMIM: "Intolerance to heat and fever" [OMIM:Intolerance to heat and fever]
UMLS:C0231274 "Intolerant of heat" [Orphanet:23020]
Is a (Direct Parents):
MedDRA Feelings and sensations NEC
HPO         Abnormality of temperature regulation
Orphanet Hypohidrosis
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of temperature regulation(HPO:0004370)
             Heat intolerance(HPO:0002046)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       Feelings and sensations NEC(MedDRA:10068759)
          Heat intolerance(HPO:0002046)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS (OMIM:106190)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
CARDIOFACIOCUTANEOUS SYNDROME 3 (OMIM:615279)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
Fabry disease (Orphanet:324)
Monosomy 22q13 (Orphanet:48652)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)