FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Rapp-Hodgkin syndrome ID (Ontology) DOID:0060330 (Human Disease)
Definition An ectodermal dysplasia characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate.
Also Known As "anhidrotic ectodermal dysplasia with cleft lip/palate" ; "ectodermal dysplasia syndrome, Rapp-Hodgkin type" ; "ectodermal dysplasia, Rapp-Hodgkin type" (for all, see Synonyms field below)
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 Genes
 Rapp-Hodgkin syndrome       1
 for disease ribbon | Rapp-Hodgkin syndrome       1
 model of | Rapp-Hodgkin syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
 |__ectodermal dysplasia________|
                                Rapp-Hodgkin syndrome  1 rec.
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Is a autosomal dominant disease
ectodermal dysplasia
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Synonyms
  • "anhidrotic ectodermal dysplasia with cleft lip/palate" EXACT
    "ectodermal dysplasia syndrome, Rapp-Hodgkin type" EXACT
    "ectodermal dysplasia, Rapp-Hodgkin type" EXACT
    "RHS" EXACT OMO:0003012
Secondary IDs
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GARD:5690
MESH:C535289
MIM:129400
ORDO:3022