Hypohidrosis
Symptom Information:
Symptom ID: | HPO:0000966 | |||||||||||||||||
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 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) |
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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) |