MeSH Browser

MeSH Heading: Ectodermal Dysplasia
Tree Number(s): C16.131.077.350; C16.131.831.350; C16.320.850.250; C17.800.804.350; C17.800.827.250
Unique ID: D004476
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D004476
Scope Note: A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
Entry Term(s): Anhidrotic Ectodermal Dysplasia; Anhydrotic Ectodermal Dysplasia; Aplasia Cutis Congenita; Aplasia Cutis Congenita, Nonsyndromic; Autosomal Dominant Hidrotic Ectodermal Dysplasia; Clouston Hidrotic Ectodermal Dysplasia; Clouston Syndrome; Clouston's Hidrotic Ectodermal Dysplasia; Clouston's Syndrome; Congenital Ectodermal Defect; Defect, Congenital Ectodermal; Ectodermal Defect, Congenital; Ectodermal Dysplasia 2, Hidrotic; Ectodermal Dysplasia Anhidrotic; Ectodermal Dysplasia, Anhydrotic; Ectodermal Dysplasia, Hidrotic; Ectodermal Dysplasia, Hidrotic, Autosomal Dominant; Hidrotic Ectodermal Dysplasia; Hidrotic Ectodermal Dysplasia, Autosomal Dominant; Hydrotic Ectodermal Dysplasia
NLM Classification #: WR 218
Public MeSH Note: 1965; ECTODERMAL DEFECT, CONGENITAL was heading 1963-1986
History Note: 1965
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2015/06/18

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Abnormalities, Multiple [C16.131.077]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Skin Abnormalities [C16.131.831]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Skin Diseases, Genetic [C16.320.850]

Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
  - Skin Abnormalities [C17.800.804]

Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
  - Skin Diseases, Genetic [C17.800.827]

Ectodermal Dysplasia Preferred

Concept UI: M0007032
Scope Note: A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
Terms: Ectodermal Dysplasia Preferred Term
Term UI T013665
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1965); Congenital Ectodermal Defect
Term UI T013662
Date04/30/1986
LexicalTag NON
ThesaurusID UNK (19XX); Defect, Congenital Ectodermal
Term UI T013663
Date04/30/1986
LexicalTag NON
ThesaurusID UNK (19XX); Ectodermal Defect, Congenital
Term UI T013664
Date04/03/1986
LexicalTag NON
ThesaurusID UNK (19XX)

Hidrotic Ectodermal Dysplasia Narrower

Aplasia Cutis Congenita Narrower

Anhidrotic Ectodermal Dysplasia Narrower

Ectodermal Dysplasia MeSH Descriptor Data 2024