Hypohidrosis

Symptom Information:

Symptom ID: HPO:0000966
Synonyms:
Decreased ability to sweat [HPO:0000966]
Decreased sweating [HPO:0000966]
Oligohidrosis [HPO:0000966]
Hypohidrosis (disorder) [Orphanet:23020]
Diminished sweating (finding) [Orphanet:23020]
Hypohidrosis [Orphanet:23020]
Diminished sweating [Orphanet:23020]
Decreased ability to sweat [OMIM:Decreased ability to sweat]
Decreased sweating [OMIM:Decreased sweating]
Hypohidrosis [OMIM:Hypohidrosis]
Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance [Orphanet:23020]
Sweating decreased [Orphanet:23020]
Hypohidrosis [MedDRA:10021013]
Hyphidrosis [MedDRA:10021013]
Sweating decreased [MedDRA:10021013]
Hypohidrosis (in most patients) [OMIM:Hypohidrosis (in most patients)]
Hypohidrosis (in some patients) [OMIM:Hypohidrosis (in some patients)]
Quality:
Cross references:
HPO:0007500 "Decreased number of sweat glands" [Orphanet:23020]
Orphanet:23020 "Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance" [Orphanet:23020]
OMIM: "Decreased ability to sweat" [OMIM:Decreased ability to sweat]
OMIM: "Decreased sweating" [OMIM:Decreased sweating]
OMIM: "Hypohidrosis" [OMIM:Hypohidrosis]
OMIM: "Hypohidrosis (in most patients)" [OMIM:Hypohidrosis (in most patients)]
OMIM: "Hypohidrosis (in some patients)" [OMIM:Hypohidrosis (in some patients)]
UMLS:C0020620 "Hypohidrosis" [HPO:0000966]
UMLS:C0020620 "Hypohidrosis" [Orphanet:23020]
UMLS:C0553721 "Diminished sweating" [Orphanet:23020]
Is a (Direct Parents):
HPO         Abnormality of the sweat gland
Orphanet Abnormality of the skin
MedDRA General signs and symptoms NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the sweat gland(HPO:0000971)
                Hypohidrosis(HPO:0000966)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       General signs and symptoms NEC(MedDRA:10018072)
          Hypohidrosis(HPO:0000966)
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
AREDYLD syndrome (Orphanet:1133)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Bazex-Dupré-Christol syndrome (Orphanet:113)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
Fabry disease (Orphanet:324)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Generalized basaloid follicular hamartoma syndrome (Orphanet:168632)
HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES (OMIM:241120)
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome (Orphanet:363523)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 (OMIM:242100)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3 (OMIM:606545)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
KID syndrome (Orphanet:477)
Limb-mammary syndrome (Orphanet:69085)
MYXEDEMA (OMIM:255900)
Monosomy 22q13 (Orphanet:48652)
Multiple system atrophy (Orphanet:102)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS (OMIM:615704)
Polyneuropathy - hand defect (Orphanet:2926)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Rosselli-Gulienetti syndrome (Orphanet:90339)
Sandhoff disease, infantile form (Orphanet:309155)
Self-healing collodion baby (Orphanet:281122)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Wolfram syndrome 1 (OMIM:222300)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked intellectual deficit, Najm type (Orphanet:163937)