Hypohidrotic ectodermal dysplasia

Symptom Information:

Symptom ID: HPO:0007607
Synonyms:
Hypohidrotic ectodermal dysplasia [OMIM:Hypohidrotic ectodermal dysplasia]
Quality:
Cross references:
OMIM: "Hypohidrotic ectodermal dysplasia" [OMIM:Hypohidrotic ectodermal dysplasia]
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)
                   Hypohidrotic ectodermal dysplasia(HPO:0007607)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT (OMIM:614940)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)