Anhidrotic ectodermal dysplasia

Symptom Information:

Symptom ID: HPO:0007476
Synonyms:
Anhidrotic ectodermal dysplasia [OMIM:Anhidrotic ectodermal dysplasia]
Ectodermal dysplasia, anhidrotic [OMIM:Ectodermal dysplasia, anhidrotic]
Quality:
Cross references:
OMIM: "Anhidrotic ectodermal dysplasia" [OMIM:Anhidrotic ectodermal dysplasia]
OMIM: "Ectodermal dysplasia, anhidrotic" [OMIM:Ectodermal dysplasia, anhidrotic]
Is a (Direct Parents):
HPO         Ectodermal dysplasia
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:
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)