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Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
MeSH HeadingEctodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Tree NumberC16.131.077.350.348
Tree NumberC16.131.831.350.348
Tree NumberC16.320.850.250.348
Tree NumberC17.800.804.350.348
Tree NumberC17.800.827.250.348
Scope NoteAn autosomal recessive form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR or EDAR-ASSOCIATED DEATH DOMAIN PROTEIN.
Entry TermAnhidridic Ectodermal Dysplasia, Autosomal Recessive
Entry TermAnhydridic Ectodermal Dysplasia, Autosomal Recessive
Entry TermAutosomal Recessive Anhidrotic Ectodermal Dysplasia
Entry TermAutosomal Recessive Anhydrotic Ectodermal Dysplasia
Entry TermEctodermal Dysplasia, Anhidrotic, Autosomal Recessive
Entry TermEctodermal Dysplasia, Hypohydrotic, Autosomal Recessive
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UL UR US VE VI
Previous Indexing Ectodermal Dysplasia (1971-2006)
History Note2007
Date of Entry20060705
Unique IDD053360


MeSH Tree Structures

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Abnormalities, Multiple [C16.131.077]
         Ectodermal Dysplasia [C16.131.077.350]
Ectodermal Dysplasia 1, Anhidrotic [C16.131.077.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.131.077.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.131.077.350.348]
Ellis-Van Creveld Syndrome [C16.131.077.350.398]
Focal Dermal Hypoplasia [C16.131.077.350.424]
Neurocutaneous Syndromes [C16.131.077.350.712]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Skin Abnormalities [C16.131.831]
         Ectodermal Dysplasia [C16.131.831.350]
Ectodermal Dysplasia 1, Anhidrotic [C16.131.831.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.131.831.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.131.831.350.348]
Ellis-Van Creveld Syndrome [C16.131.831.350.398]
Focal Dermal Hypoplasia [C16.131.831.350.424]
Neurocutaneous Syndromes [C16.131.831.350.712]
Pachyonychia Congenita [C16.131.831.350.856]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Skin Diseases, Genetic [C16.320.850]
         Ectodermal Dysplasia [C16.320.850.250]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.850.250.198]
Ectodermal Dysplasia 3, Anhidrotic [C16.320.850.250.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C16.320.850.250.348]
Ellis-Van Creveld Syndrome [C16.320.850.250.398]
Focal Dermal Hypoplasia [C16.320.850.250.424]
Neurocutaneous Syndromes [C16.320.850.250.712]
Pachyonychia Congenita [C16.320.850.250.856]

 
Skin and Connective Tissue Diseases [C17]
   Skin Diseases [C17.800]
      Skin Abnormalities [C17.800.804]
         Ectodermal Dysplasia [C17.800.804.350]
Ectodermal Dysplasia 1, Anhidrotic [C17.800.804.350.198]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.804.350.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.804.350.348]
Ellis-Van Creveld Syndrome [C17.800.804.350.398]
Focal Dermal Hypoplasia [C17.800.804.350.424]
Neurocutaneous Syndromes [C17.800.804.350.712]
Pachyonychia Congenita [C17.800.804.350.856]

 
Skin and Connective Tissue Diseases [C17]
   Skin Diseases [C17.800]
      Skin Diseases, Genetic [C17.800.827]
         Ectodermal Dysplasia [C17.800.827.250]
Ectodermal Dysplasia 1, Anhidrotic [C17.800.827.250.198]
Ectodermal Dysplasia 3, Anhidrotic [C17.800.827.250.298]
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [C17.800.827.250.348]
Ellis-Van Creveld Syndrome [C17.800.827.250.398]
Focal Dermal Hypoplasia [C17.800.827.250.424]
Neurocutaneous Syndromes [C17.800.827.250.712]
Pachyonychia Congenita [C17.800.827.250.856]

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