Ectodermal Dysplasia [ektodermální dysplazie]

topical
33
Terms

anhidrotická ektodermální dysplazie
aplasia cutis congenita
Cloustonův syndrom
hidrotická ektodermální dysplazie
vrozená ektodermální dysplazie

 

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

Persistent link   https://www.medvik.cz/link/D004476
Definition

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.

DUI
D004476 MeSH Browser
CUI
M0007032
History note
1965
Public note
1965; ECTODERMAL DEFECT, CONGENITAL was heading 1963-1986

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 3
CO
complications 6
DI
diagnosis 11
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 1
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 8
GE
genetics 15
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 4
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 8
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.077 Abnormalities, Multiple 330
C16.131.077.019 22q11 Deletion Syndrome 2
C16.131.077.065 Alagille Syndrome 19
C16.131.077.095 Angelman Syndrome 35
C16.131.077.121 Barth Syndrome 6
C16.131.077.130 Basal Cell Nevus Syndrome 33
C16.131.077.133 Beckwith-Wiedemann Syndrome 17
C16.131.077.137 Bloom Syndrome 11
C16.131.077.208 Branchio-Oto-Renal Syndrome 5
C16.131.077.229 Carney Complex 8
C16.131.077.245 Ciliopathies 9
C16.131.077.250 Cockayne Syndrome 4
C16.131.077.256 Costello Syndrome 3
C16.131.077.262 Cri-du-Chat Syndrome 11
C16.131.077.272 De Lange Syndrome 4
C16.131.077.299 Deaf-Blind Disorders 65
C16.131.077.313 Donohue Syndrome 1
C16.131.077.327 Down Syndrome 510
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.131.077.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.131.077.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.131.077.350.398 Ellis-Van Creveld Syndrome 11
C16.131.077.350.424 Focal Dermal Hypoplasia 6
C16.131.077.350.568 Focal Facial Dermal Dysplasias
C16.131.077.350.712 Neurocutaneous Syndromes 30
C16.131.077.350.856 Pachyonychia Congenita 3
C16.131.077.371 Fraser Syndrome 2
C16.131.077.393 Gardner Syndrome 21
C16.131.077.401 Heterotaxy Syndrome 7
C16.131.077.410 Holoprosencephaly 9
C16.131.077.445 Incontinentia Pigmenti 19
C16.131.077.477 Isolated Noncompaction of the Ventricular Myocardium 11
C16.131.077.509 Laurence-Moon Syndrome 6
C16.131.077.525 LEOPARD Syndrome 11
C16.131.077.537 Loeys-Dietz Syndrome 7
C16.131.077.550 Marfan Syndrome 105
C16.131.077.578 Mobius Syndrome 10
C16.131.077.592 Monilethrix 1
C16.131.077.606 Nail-Patella Syndrome 8
C16.131.077.619 Netherton Syndrome 2
C16.131.077.633 Nevus, Sebaceous of Jadassohn 7
C16.131.077.662 Oculocerebrorenal Syndrome 9
C16.131.077.676 Orofaciodigital Syndromes 7
C16.131.077.690 Pallister-Hall Syndrome
C16.131.077.696 Pentalogy of Cantrell 1
C16.131.077.703 POEMS Syndrome 35
C16.131.077.717 Polycystic Kidney Diseases 83
C16.131.077.730 Prader-Willi Syndrome 92
C16.131.077.735 Prolidase Deficiency
C16.131.077.740 Proteus Syndrome 8
C16.131.077.745 Prune Belly Syndrome 3
C16.131.077.790 Rubella Syndrome, Congenital 20
C16.131.077.804 Rubinstein-Taybi Syndrome 12
C16.131.077.850 Short Rib-Polydactyly Syndrome 3
C16.131.077.855 Silver-Russell Syndrome 3
C16.131.077.860 Smith-Lemli-Opitz Syndrome 30
C16.131.077.879 Smith-Magenis Syndrome 2
C16.131.077.889 Sotos Syndrome 4
C16.131.077.899 Trichothiodystrophy Syndromes 1
C16.131.077.919 Trisomy 13 Syndrome 6
C16.131.077.929 Trisomy 18 Syndrome 5
C16.131.077.938 Waardenburg Syndrome 10
C16.131.077.941 Weill-Marchesani Syndrome 1
C16.131.077.944 Wolf-Hirschhorn Syndrome
C16.131.077.970 Zellweger Syndrome 10
C16.131.831 Skin Abnormalities 51
C16.131.831.066 Acrodermatitis 67
C16.131.831.108 Carney Complex 8
C16.131.831.150 Dyskeratosis Congenita 9
C16.131.831.350 Ectodermal Dysplasia 33
C16.131.831.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.131.831.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.131.831.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.131.831.350.398 Ellis-Van Creveld Syndrome 11
C16.131.831.350.424 Focal Dermal Hypoplasia 6
C16.131.831.350.568 Focal Facial Dermal Dysplasias
C16.131.831.350.712 Neurocutaneous Syndromes 30
C16.131.831.350.856 Pachyonychia Congenita 3
C16.131.831.428 Ehlers-Danlos Syndrome 51
C16.131.831.493 Epidermolysis Bullosa 108
C16.131.831.512 Ichthyosis 62
C16.131.831.580 Incontinentia Pigmenti 19
C16.131.831.675 Port-Wine Stain 5
C16.131.831.720 Prolidase Deficiency
C16.131.831.766 Pseudoxanthoma Elasticum 13
C16.131.831.775 Rothmund-Thomson Syndrome 8
C16.131.831.812 Sclerema Neonatorum 2
C16.131.831.874 Trichothiodystrophy Syndromes 1
C16.131.831.936 Xeroderma Pigmentosum 25
C16.320 Genetic Diseases, Inborn 1 215
C16.320.850 Skin Diseases, Genetic 89
C16.320.850.080 Albinism 17
C16.320.850.180 Cutis Laxa 10
C16.320.850.190 Darier Disease 26
C16.320.850.210 Dermatitis, Atopic 1 454
C16.320.850.235 Dyskeratosis Congenita 9
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.250.198 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.850.250.298 Ectodermal Dysplasia 3, Anhidrotic 1
C16.320.850.250.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C16.320.850.250.398 Ellis-Van Creveld Syndrome 11
C16.320.850.250.424 Focal Dermal Hypoplasia 6
C16.320.850.250.568 Focal Facial Dermal Dysplasias
C16.320.850.250.712 Neurocutaneous Syndromes 30
C16.320.850.250.856 Pachyonychia Congenita 3
C16.320.850.260 Ehlers-Danlos Syndrome 51
C16.320.850.275 Epidermolysis Bullosa 108
C16.320.850.337 Erythrokeratodermia Variabilis 1
C16.320.850.368 Hyaline Fibromatosis Syndrome 1
C16.320.850.400 Ichthyosiform Erythroderma, Congenital 8
C16.320.850.402 Ichthyosis Bullosa of Siemens 3
C16.320.850.405 Ichthyosis Vulgaris 5
C16.320.850.408 Ichthyosis, X-Linked 9
C16.320.850.420 Incontinentia Pigmenti 19
C16.320.850.475 Keratoderma, Palmoplantar 15
C16.320.850.542 Leukokeratosis, Hereditary Mucosal 1
C16.320.850.595 Lipoid Proteinosis of Urbach and Wiethe 5
C16.320.850.647 Monilethrix 1
C16.320.850.673 Netherton Syndrome 2
C16.320.850.700 Pemphigus, Benign Familial 11
C16.320.850.730 Porokeratosis 11
C16.320.850.738 Porphyria, Erythropoietic 11
C16.320.850.742 Porphyrias, Hepatic 27
C16.320.850.746 Prolidase Deficiency
C16.320.850.750 Pseudoxanthoma Elasticum 13
C16.320.850.765 Rothmund-Thomson Syndrome 8
C16.320.850.820 Sjogren-Larsson Syndrome 4
C16.320.850.895 Trichothiodystrophy Syndromes 1
C16.320.850.970 Xeroderma Pigmentosum 25
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 801
C17.800.804 Skin Abnormalities 51
C17.800.804.066 Acrodermatitis 67
C17.800.804.108 Anetoderma 5
C17.800.804.150 Dyskeratosis Congenita 9
C17.800.804.350 Ectodermal Dysplasia 33
C17.800.804.350.198 Ectodermal Dysplasia 1, Anhidrotic 3
C17.800.804.350.298 Ectodermal Dysplasia 3, Anhidrotic 1
C17.800.804.350.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C17.800.804.350.398 Ellis-Van Creveld Syndrome 11
C17.800.804.350.424 Focal Dermal Hypoplasia 6
C17.800.804.350.568 Focal Facial Dermal Dysplasias
C17.800.804.350.712 Neurocutaneous Syndromes 30
C17.800.804.350.856 Pachyonychia Congenita 3
C17.800.804.428 Ehlers-Danlos Syndrome 51
C17.800.804.493 Epidermolysis Bullosa 108
C17.800.804.512 Ichthyosis 62
C17.800.804.580 Incontinentia Pigmenti 19
C17.800.804.675 Port-Wine Stain 5
C17.800.804.766 Pseudoxanthoma Elasticum 13
C17.800.804.775 Rothmund-Thomson Syndrome 8
C17.800.804.812 Sclerema Neonatorum 2
C17.800.804.874 Trichothiodystrophy Syndromes 1
C17.800.804.936 Xeroderma Pigmentosum 25
C17.800.827 Skin Diseases, Genetic 89
C17.800.827.080 Albinism 17
C17.800.827.180 Cutis Laxa 10
C17.800.827.190 Darier Disease 26
C17.800.827.210 Dermatitis, Atopic 1 454
C17.800.827.235 Dyskeratosis Congenita 9
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.250.198 Ectodermal Dysplasia 1, Anhidrotic 3
C17.800.827.250.298 Ectodermal Dysplasia 3, Anhidrotic 1
C17.800.827.250.348 Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 2
C17.800.827.250.398 Ellis-Van Creveld Syndrome 11
C17.800.827.250.424 Focal Dermal Hypoplasia 6
C17.800.827.250.568 Focal Facial Dermal Dysplasias
C17.800.827.250.712 Neurocutaneous Syndromes 30
C17.800.827.250.856 Pachyonychia Congenita 3
C17.800.827.260 Ehlers-Danlos Syndrome 51
C17.800.827.275 Epidermolysis Bullosa 108
C17.800.827.337 Erythrokeratodermia Variabilis 1
C17.800.827.368 Hereditary Autoinflammatory Diseases 47
C17.800.827.384 Hyaline Fibromatosis Syndrome 1
C17.800.827.400 Ichthyosiform Erythroderma, Congenital 8
C17.800.827.403 Ichthyosis Bullosa of Siemens 3
C17.800.827.405 Ichthyosis Vulgaris 5
C17.800.827.408 Ichthyosis, X-Linked 9
C17.800.827.420 Incontinentia Pigmenti 19
C17.800.827.475 Keratoderma, Palmoplantar 15
C17.800.827.595 Leukokeratosis, Hereditary Mucosal 1
C17.800.827.602 Monilethrix 1
C17.800.827.610 Muir-Torre Syndrome 10
C17.800.827.655 Netherton Syndrome 2
C17.800.827.700 Pemphigus, Benign Familial 11
C17.800.827.730 Porokeratosis 11
C17.800.827.738 Porphyria, Erythropoietic 11
C17.800.827.742 Porphyrias, Hepatic 27
C17.800.827.750 Pseudoxanthoma Elasticum 13
C17.800.827.775 Rothmund-Thomson Syndrome 8
C17.800.827.820 Sjogren-Larsson Syndrome 4
C17.800.827.895 Trichothiodystrophy Syndromes 1
C17.800.827.970 Xeroderma Pigmentosum 25

AREDYLD Syndrome Disease MeSH Browser

Adams Oliver syndrome Disease MeSH Browser

Alves Castelo dos Santos syndrome Disease MeSH Browser

Anal sphincter dysplasia Disease MeSH Browser

Aplasia Cutis Congenita with Epibulbar Dermoids Disease MeSH Browser

Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts Disease MeSH Browser

Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction Disease MeSH Browser

Aplasia cutis congenita intestinal lymphangiectasia Disease MeSH Browser

Aplasia cutis congenita of limbs recessive Disease MeSH Browser

Arthrogryposis and ectodermal dysplasia Disease MeSH Browser

Basan syndrome Disease MeSH Browser

Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Disease MeSH Browser

Brunoni syndrome Disease MeSH Browser

Cardiofaciocutaneous syndrome Disease MeSH Browser

Cerebellar ataxia ectodermal dysplasia Disease MeSH Browser

Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 Disease MeSH Browser

Congenital ectodermal dysplasia with hearing loss Disease MeSH Browser

Contractures ectodermal dysplasia cleft lip palate Disease MeSH Browser

Cranioectodermal Dysplasia Disease MeSH Browser

Deafness with Anhidrotic Ectodermal Dysplasia Disease MeSH Browser

Dermatoosteolysis Kirghizian type Disease MeSH Browser

Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet Disease MeSH Browser

Ectodermal Dysplasia and Neurosensory Deafness Disease MeSH Browser

Ectodermal Dysplasia with Natal Teeth, Turnpenny Type Disease MeSH Browser

Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Disease MeSH Browser

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Disease MeSH Browser

Ectodermal Dysplasia, Hidrotic, Autosomal Recessive Disease MeSH Browser

Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum Disease MeSH Browser

Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia Disease MeSH Browser

Ectodermal Dysplasia, Pure Hair-Nail Type Disease MeSH Browser

Ectodermal Dysplasia, Trichoodontoonychial Type Disease MeSH Browser

Ectodermal Dysplasia-Skin Fragility Syndrome Disease MeSH Browser

Ectodermal dysplasia adrenal cyst Disease MeSH Browser

Ectodermal dysplasia alopecia preaxial polydactyly Disease MeSH Browser

Ectodermal dysplasia mental retardation syndactyly Disease MeSH Browser

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Disease MeSH Browser

Ectodermal dysplasia, hidrotic, Christianson-Fourie type Disease MeSH Browser

Ectodermal dysplasia, hypohidrotic, with immune deficiency Disease MeSH Browser

Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features Disease MeSH Browser

Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate Disease MeSH Browser

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1 Disease MeSH Browser

Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3 Disease MeSH Browser

Ectrodactyly-cleft lip-palate syndrome Disease MeSH Browser

Epidermolysis bullosa with pyloric atresia Disease MeSH Browser

Euhidrotic ectodermal dysplasia Disease MeSH Browser

Freire-Maia odontotrichomelic syndrome Disease MeSH Browser

Halal Setton Wang syndrome Disease MeSH Browser

Hay Wells syndrome recessive type Disease MeSH Browser

Hay-Wells syndrome Disease MeSH Browser

Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic Disease MeSH Browser

Johanson Blizzard syndrome Disease MeSH Browser

Jones Hersh Yusk syndrome Disease MeSH Browser

Ladda Zonana Ramer syndrome Disease MeSH Browser

Lelis Syndrome Disease MeSH Browser

Madokoro Ohdo Sonoda syndrome Disease MeSH Browser

NEMO mutation with immunodeficiency Disease MeSH Browser

Naegeli syndrome Disease MeSH Browser

Odontomicronychial dysplasia Disease MeSH Browser

Odontoonychodermal dysplasia Disease MeSH Browser

Odontotrichoungual-Digital-Palmar Syndrome Disease MeSH Browser

Orofacial Cleft 7 Disease MeSH Browser

Pinheiro Freire-Maia Miranda syndrome Disease MeSH Browser

Propping Zerres syndrome Disease MeSH Browser

Rapp-Hodgkin syndrome Disease MeSH Browser

Robinson Miller Bensimon syndrome Disease MeSH Browser

Rosselli-Gulienetti Syndrome Disease MeSH Browser

Sener syndrome Disease MeSH Browser

Seres-Santamaria Arimany Muniz syndrome Disease MeSH Browser

Taurodontia absent teeth sparse hair Disease MeSH Browser

Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities Disease MeSH Browser

Trichodental syndrome Disease MeSH Browser

Trichoodontoonychial Dysplasia Disease MeSH Browser

Trichoscyphodysplasia Disease MeSH Browser

Trueb Burg Bottani syndrome Disease MeSH Browser

Yunis Varon syndrome Disease MeSH Browser

Zlotogora-Ogur syndrome Disease MeSH Browser

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