Heat intolerance
Symptom Information:
Symptom ID: | HPO:0002046 | ||||||||||||
Synonyms: |
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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 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) |
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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) |