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Focal Dermal Hypoplasia

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia 29 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Ectodermal Dysplasia 1, Anhidrotic \| ∟ Fabry Disease \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita \| ∟ Craniofacial Dysostosis \| ∟ Klippel-Feil Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ Rubinstein-Taybi Syndrome \| ∟ Synostosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dysostoses ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Focal Dermal Hypoplasia Ectodermal Dysplasia > Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Dysostoses > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Annotation:	sometimes called Goltz-Gorlin syndrome but do not confuse with Gorlin-Goltz syndrome which is same as GORLIN SYNDROME see BASAL CELL NEVUS SYNDROME; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
History note:	Abnormalities, Multiple (1968-1984) \| Skin (1966-1984) \| Skin Diseases (1966-1984)X
historyNote*:	91(85); was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 X
onlineNote*:	use FOCAL DERMAL HYPOPLASIA to search GOLTZ-GORLIN SYNDROME 1985-92 X
publicMeSHNote*:	91; was see under ECTODERMAL DYSPLASIA 1987-90, was see under ECTODERMAL DEFECT, CONGENITAL 1985-86; GOLTZ-GORLIN SYNDROME was see FOCAL DERMAL HYPOPLASIA 1985-92 X
Scope note:	A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait. X
activeMeSHYear*:	2007X
dateCreated*:	1984-04-05X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	RCX
Type:	Concept X
Coordinate terms:	Androgen-Insensitivity Syndrome \| Choroideremia \| Dyskeratosis Congenita \| Ectodermal Dysplasia 1, Anhidrotic \| Fabry Disease \| Glycogen Storage Disease Type IIb \| Glycogen Storage Disease Type VIII \| Granulomatous Disease, Chronic \| Hemophilia B \| Hyper-IgM Immunodeficiency Syndrome, Type 1 \| Hypophosphatemic Rickets, X-Linked Dominant \| Ichthyosis, X-Linked \| Mental Retardation, X-Linked \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Oculocerebrorenal Syndrome \| Pelizaeus-Merzbacher Disease \| Wiskott-Aldrich Syndrome \| X-Linked Combined Immunodeficiency Diseases \| Ectodermal Dysplasia 3, Anhidrotic \| Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| Ellis-Van Creveld Syndrome \| Neurocutaneous Syndromes \| Pachyonychia Congenita \| Craniofacial Dysostosis \| Klippel-Feil Syndrome \| Orofaciodigital Syndromes \| Rubinstein-Taybi Syndrome \| Synostosis X
URI:	X
Labels and equivalent concepts:	Fokaalinen ihon hypoplasia (fi) Goltzin syndrooma (fi, replaced) Pesäkkeinen ihon hypoplasia (fi, replaced) Goltzin oireyhtymä (fi, replaced) Fokal hudhypoplasi (sv) Goltz's Syndrome (en, replaced) Goltz Syndrome (en, replaced) Dermal Hypoplasia, Focal (en, replaced) X
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