Decreased number of sweat glands

Symptom Information:

Symptom ID: HPO:0007500
Synonyms:
Decreased sweat glands [HPO:0007500]
Decreased sweat pores [HPO:0007500]
Hypohidrosis [Orphanet:23020]
Hypohidrosis (disorder) [Orphanet:23020]
Diminished sweating (finding) [Orphanet:23020]
Diminished sweating [Orphanet:23020]
Decreased sweat glands [OMIM:Decreased sweat glands]
Decreased sweat pores [OMIM:Decreased sweat pores]
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:0000966 "Hypohidrosis" [Orphanet:23020]
Orphanet:23020 "Hypohidrosis/decreased sweating/thermoregulation disorder/heat intolerance" [Orphanet:23020]
OMIM: "Decreased sweat glands" [OMIM:Decreased sweat glands]
OMIM: "Decreased sweat pores" [OMIM:Decreased sweat pores]
OMIM: "Hypohidrosis (in most patients)" [OMIM:Hypohidrosis (in most patients)]
OMIM: "Hypohidrosis (in some patients)" [OMIM:Hypohidrosis (in some patients)]
UMLS:C0020620 "Hypohidrosis" [Orphanet:23020]
UMLS:C0553721 "Diminished sweating" [Orphanet:23020]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA General signs and symptoms NEC
HPO         Abnormality of the sweat gland
Orphanet Hypohidrosis
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)
                Decreased number of sweat glands(HPO:0007500)
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       General signs and symptoms NEC(MedDRA:10018072)
          Decreased number of sweat glands(HPO:0007500)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES (OMIM:241120)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 (OMIM:242100)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
RAPP-HODGKIN SYNDROME (OMIM:129400)