Abnormality of temperature regulation

Symptom Information:

Symptom ID: HPO:0004370
Synonyms:
Body temperature changes [HPO:0004370]
Poor temperature regulation [HPO:0004370]
Thermoregulation disorder [Orphanet:23020]
Poor temperature regulation [OMIM:Poor temperature regulation]
Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance [Orphanet:23020]
Quality:
Cross references:
Orphanet:23020 "Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance" [Orphanet:23020]
OMIM: "Poor temperature regulation" [OMIM:Poor temperature regulation]
Is a (Direct Parents):
HPO         Abnormality of metabolism/homeostasis
Orphanet Abnormality of the skin
Orphanet Hypohidrosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of temperature regulation(HPO:0004370)
MedDRA:
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

Absence of fingerprints - congenital milia (Orphanet:1658)
Acanthosis nigricans (Orphanet:924)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Amelo-cerebro-hypohidrotic syndrome (Orphanet:1946)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Arachnoiditis (Orphanet:137817)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
CADASIL (Orphanet:136)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Congenital cataract - ichthyosis (Orphanet:1376)
Congenital non-bullous ichthyosiform erythroderma (Orphanet:79394)
Contractures - ectodermal dysplasia - cleft lip/palate (Orphanet:1484)
Cystinosis (Orphanet:213)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Dermo-odonto dysplasia (Orphanet:1660)
Disseminated superficial actinic porokeratosis (Orphanet:79152)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Erythrokeratodermia - ataxia (Orphanet:1955)
Fabry disease (Orphanet:324)
Familial dysautonomia (Orphanet:1764)
Haddad syndrome (Orphanet:99803)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
KID syndrome (Orphanet:477)
Laron syndrome (Orphanet:633)
Leigh syndrome (Orphanet:506)
Lymphangioleiomyomatosis (Orphanet:538)
MELAS (Orphanet:550)
Marshall syndrome (Orphanet:560)
Monosomy 22q13 (Orphanet:48652)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Ondine syndrome (Orphanet:661)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Polyneuropathy - hand defect (Orphanet:2926)
Recessive X-linked ichthyosis (Orphanet:461)
Rosaï-Dorfman disease (Orphanet:158014)
Scalp-ear-nipple syndrome (Orphanet:2036)
Septo-optic dysplasia (Orphanet:3157)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Stüve-Wiedemann syndrome (Orphanet:3206)
Syndromic X-linked ichthyosis (Orphanet:281090)
Teebi-Shaltout syndrome (Orphanet:3291)
Tetrasomy 12p (Orphanet:884)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Ulnar-mammary syndrome (Orphanet:3138)
Van den Bosch syndrome (Orphanet:3417)
Wolfram syndrome 1 (OMIM:222300)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Zlotogora-Ogur syndrome (Orphanet:3253)