Neurocutaneous Syndromes [neurokutánní syndromy]

topical
29
Terms

fakomatóza
fakomatózy
neuroektodermální dysplastické syndromy

 

Neurocutaneous Disorders
Neuroectodermal Dysplasia Syndromes
Phacomatoses
Phacomatosis
Phakomatoses
Phakomatosis

Persistent link   https://www.medvik.cz/link/D020752
Definition

A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs.

Annotation
for neurocutaneous melanosis, coord with MELANOSIS
DUI
D020752 MeSH Browser
CUI
M0328284
Previous indexing
Abnormalities, Multiple (1966-1999); Nervous System Diseases (1967-1999); Skin Diseases (1967-1999)
History note
2000
Public note
2000

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 6
CO
complications 4
CN
congenital 1
DI
diagnosis 15
DG
diagnostic imaging 1
DH
diet therapy
DT
drug therapy 3
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 1
EH
ethnology
ET
etiology 4
GE
genetics 4
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 7
PP
physiopathology 2
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 5
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 878
C10.114 Autoimmune Diseases of the Nervous System 94
C10.177 Autonomic Nervous System Diseases 138
C10.228 Central Nervous System Diseases 808
C10.281 Chronobiology Disorders 34
C10.292 Cranial Nerve Diseases 60
C10.314 Demyelinating Diseases 305
C10.500 Nervous System Malformations 80
C10.551 Nervous System Neoplasms 81
C10.562 Neurocutaneous Syndromes 29
C10.562.100 Ataxia Telangiectasia 47
C10.562.600 Neurofibromatoses 28
C10.562.700 Nevus, Sebaceous of Jadassohn 7
C10.562.800 Sturge-Weber Syndrome 25
C10.562.850 Tuberous Sclerosis 141
C10.562.925 von Hippel-Lindau Disease 56
C10.574 Neurodegenerative Diseases 641
C10.586 Neuroinflammatory Diseases 17
C10.597 Neurologic Manifestations 1 052
C10.668 Neuromuscular Diseases 330
C10.720 Neurotoxicity Syndromes 148
C10.803 Restless Legs Syndrome 190
C10.886 Sleep Wake Disorders 1 177
C10.900 Trauma, Nervous System 62
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.077 Abnormalities, Multiple 330
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 29
C16.131.077.350.856 Pachyonychia Congenita 3
C16.131.831 Skin Abnormalities 51
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 29
C16.131.831.350.856 Pachyonychia Congenita 3
C16.320 Genetic Diseases, Inborn 1 213
C16.320.850 Skin Diseases, Genetic 89
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 29
C16.320.850.250.856 Pachyonychia Congenita 3
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 799
C17.800.804 Skin Abnormalities 51
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 29
C17.800.804.350.856 Pachyonychia Congenita 3
C17.800.827 Skin Diseases, Genetic 89
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 29
C17.800.827.250.856 Pachyonychia Congenita 3

Angioma hereditary neurocutaneous Disease MeSH Browser

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Disease MeSH Browser

Elejalde Disease Disease MeSH Browser

Encephalocraniocutaneous lipomatosis Disease MeSH Browser

Gomez Lopez Hernandez syndrome Disease MeSH Browser

Johnson neuroectodermal syndrome Disease MeSH Browser

Neurocutaneous melanosis Disease MeSH Browser

PHACE association Disease MeSH Browser

Phacomatosis pigmentovascularis Disease MeSH Browser

Wyburn Mason's syndrome Disease MeSH Browser

Zunich neuroectodermal syndrome Disease MeSH Browser

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