Skin Diseases, Genetic [genetická onemocnění kůže]

topical
89
Terms

genetické nemoci kůže
genodermatózy
kůže - nemoci genetické
onemocnění kůže geneticky podmíněné

 

Genetic Skin Diseases

Persistent link   https://www.medvik.cz/link/D012873
Definition

Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.

Annotation
general or unspecified; prefer specifics
DUI
D012873 MeSH Browser
CUI
M0019934
Previous indexing
Skin Diseases (1975-1997)
History note
98; use explode 1970-97
Public note
98

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 9
CO
complications 1
DI
diagnosis 25
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 7
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 2
EH
ethnology
ET
etiology 6
GE
genetics 16
HI
history 2
IM
immunology 1
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 10
PP
physiopathology 6
PC
prevention & control 3
PX
psychology 1
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 11
UR
urine
VE
veterinary 1
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 214
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 47
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 259
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 57
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 46
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 5
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 711
C16.320.577 Muscular Dystrophies 140
C16.320.590 Myasthenic Syndromes, Congenital 20
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
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 1 452
C16.320.850.235 Dyskeratosis Congenita 9
C16.320.850.250 Ectodermal Dysplasia 33
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
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 800
C17.800.030 Acneiform Eruptions 33
C17.800.060 Angiolymphoid Hyperplasia with Eosinophilia 6
C17.800.090 Breast Diseases 349
C17.800.113 Calcinosis Cutis
C17.800.135 Cutaneous Fistula 26
C17.800.174 Dermatitis 332
C17.800.185 Dermatomyositis 240
C17.800.229 Erythema 200
C17.800.257 Exanthema 303
C17.800.271 Facial Dermatoses 131
C17.800.321 Foot Diseases 209
C17.800.329 Hair Diseases 174
C17.800.338 Hand Dermatoses 55
C17.800.417 Keratoacanthoma 24
C17.800.428 Keratosis 133
C17.800.446 Leg Dermatoses 25
C17.800.463 Lipomatosis 36
C17.800.480 Lupus Erythematosus, Cutaneous 77
C17.800.518 Morgellons Disease
C17.800.529 Nail Diseases 178
C17.800.550 Necrobiotic Disorders 3
C17.800.551 Necrolytic Migratory Erythema 1
C17.800.553 Nephrogenic Fibrosing Dermopathy 11
C17.800.566 Panniculitis 43
C17.800.600 Photosensitivity Disorders 188
C17.800.621 Pigmentation Disorders 132
C17.800.674 Prurigo 18
C17.800.685 Pruritus 268
C17.800.695 Pyoderma 68
C17.800.716 Rosacea 140
C17.800.738 Scalp Dermatoses 37
C17.800.751 Scleredema Adultorum 8
C17.800.767 Scleroderma, Localized 62
C17.800.784 Scleroderma, Systemic 486
C17.800.794 Sebaceous Gland Diseases 17
C17.800.804 Skin Abnormalities 51
C17.800.815 Skin Diseases, Eczematous 61
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 1 452
C17.800.827.235 Dyskeratosis Congenita 9
C17.800.827.250 Ectodermal Dysplasia 33
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 46
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
C17.800.838 Skin Diseases, Infectious 318
C17.800.849 Skin Diseases, Metabolic 17
C17.800.859 Skin Diseases, Papulosquamous 46
C17.800.862 Skin Diseases, Vascular 29
C17.800.865 Skin Diseases, Vesiculobullous 133
C17.800.882 Skin Neoplasms 1 657
C17.800.893 Skin Ulcer 139
C17.800.946 Sweat Gland Diseases 6
C17.800.973 Xanthogranuloma, Juvenile 25

Actinic Prurigo Disease MeSH Browser

Amyloidosis, Cutaneous Bullous Disease MeSH Browser

Amyloidosis, Primary Cutaneous Disease MeSH Browser

Annular Erythema Disease MeSH Browser

Arterial Tortuosity Syndrome Disease MeSH Browser

Atrophia Maculosa Varioliformis Cutis, Familial Disease MeSH Browser

Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant Disease MeSH Browser

Buschke-Ollendorff syndrome Disease MeSH Browser

Collagenosis, Familial Reactive Perforating Disease MeSH Browser

Dowling-Degos Disease Disease MeSH Browser

Dyschromatosis Universalis Hereditaria 1 Disease MeSH Browser

Dyschromatosis Universalis Hereditaria 2 Disease MeSH Browser

Dyschromatosis universalis hereditaria Disease MeSH Browser

Erythrokeratodermia with ataxia Disease MeSH Browser

Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like Disease MeSH Browser

Fingerprints, Absence of Disease MeSH Browser

Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts Disease MeSH Browser

Gerodermia osteodysplastica Disease MeSH Browser

Histiocytic Dermatoarthritis Disease MeSH Browser

Hyaluronan Metabolism, Defect in Disease MeSH Browser

Juvenile Spring Eruption of Ears Disease MeSH Browser

Keratolytic winter erythema Disease MeSH Browser

Keratosis Follicularis Spinulosa Decalvans, X-Linked Disease MeSH Browser

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Disease MeSH Browser

Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis Disease MeSH Browser

Noduli Cutanei, Multiple, with Urinary Tract Abnormalities Disease MeSH Browser

Oculotrichodysplasia Disease MeSH Browser

Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair Disease MeSH Browser

Orofaciodigital syndrome 9 Disease MeSH Browser

Osseous Heteroplasia, Progressive Disease MeSH Browser

Osteopoikilosis, Isolated Disease MeSH Browser

Parana Hard Skin Syndrome Disease MeSH Browser

Peeling Skin Syndrome Disease MeSH Browser

Perifolliculitis Capitis Abscedens Et Suffodiens, Familial Disease MeSH Browser

Pigmentary Disorder, Reticulate, with Systemic Manifestations Disease MeSH Browser

Plasminogen Deficiency, Type I Disease MeSH Browser

Poikiloderma, Hereditary Sclerosing Disease MeSH Browser

Skin Fragility-Woolly Hair Syndrome Disease MeSH Browser

Stiff Skin Syndrome Disease MeSH Browser

Storm Syndrome Disease MeSH Browser

VEXAS syndrome Disease MeSH Browser

Vitiligo, Progressive, with Mental Retardation and Urethral Duplication Disease MeSH Browser

Vohwinkel Syndrome, Variant Form Disease MeSH Browser

amyloidosis IX Disease MeSH Browser

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