Anhidrotic ectodermal dysplasia
Symptom Information:
Symptom ID: | HPO:0007476 | ||
Synonyms: |
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Quality: | |||
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 the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Ectodermal dysplasia(HPO:0000968) Anhidrotic ectodermal dysplasia(HPO:0007476) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined immunodeficiency due to ORAI1 deficiency | (Orphanet:317428) |
DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA | (OMIM:125050) |
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |