Anhidrosis
Symptom Information:
| Symptom ID: | HPO:0000970 | ||||
| Synonyms: |
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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) Anhidrosis(HPO:0000970) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Apocrine and eccrine gland disorders(MedDRA:10002982) Anhidrosis(HPO:0000970) |
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| Database Frequency: | 24 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS | (OMIM:206600) |
| ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS | (OMIM:106190) |
| Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
| Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
| Björnstad syndrome | (Orphanet:123) |
| COCKAYNE SYNDROME A | (OMIM:216400) |
| COCKAYNE SYNDROME B | (OMIM:133540) |
| Cockayne syndrome | (Orphanet:191) |
| ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:224900) |
| ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT | (OMIM:614940) |
| ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:614941) |
| ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
| Fabry disease | (Orphanet:324) |
| Fucosidosis | (Orphanet:349) |
| Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
| Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
| Hereditary sensory and autonomic neuropathy type 5 | (Orphanet:64752) |
| Multiple system atrophy | (Orphanet:102) |
| NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA | (OMIM:608720) |
| NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC | (OMIM:613640) |
| SPLENOMEGALY, CYTOPENIA, AND VISION LOSS | (OMIM:614979) |
| Van den Bosch syndrome | (Orphanet:3417) |
| Wolfram syndrome 1 | (OMIM:222300) |
| X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |