Ellis-Van Creveld Syndrome [Ellisův-van Creveldův syndrom]

topical
11
Terms

chondroektodermální dysplazie
Creveldův syndrom
ektodermální chondrodysplazie
Kauffmannův syndrom

 

Chondroectodermal Dysplasia
Ellis-Van Creveld Dysplasia
Mesoectodermal Dysplasia

Persistent link   https://www.medvik.cz/link/D004613
Definition

Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed)

Annotation
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D004613 MeSH Browser
CUI
M0007241
History note
65(63)
Public note
65

Allowable subheadings

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

C Diseases
C05 Musculoskeletal Diseases 1 125
C05.116 Bone Diseases 796
C05.116.099 Bone Diseases, Developmental 293
C05.116.099.708 Osteochondrodysplasias 125
C05.116.099.708.017 Achondroplasia 71
C05.116.099.708.025 Acquired Hyperostosis Syndrome 21
C05.116.099.708.180 Camurati-Engelmann Syndrome 6
C05.116.099.708.195 Chondrodysplasia Punctata 6
C05.116.099.708.207 Cleidocranial Dysplasia 7
C05.116.099.708.327 Ellis-Van Creveld Syndrome 11
C05.116.099.708.338 Enchondromatosis 13
C05.116.099.708.375 Fibrous Dysplasia of Bone 47
C05.116.099.708.479 Hyperostosis, Cortical, Congenital 14
C05.116.099.708.486 Hyperostosis Frontalis Interna 3
C05.116.099.708.534 Kashin-Beck Disease
C05.116.099.708.582 Langer-Giedion Syndrome 7
C05.116.099.708.670 Osteochondroma 16
C05.116.099.708.685 Osteogenesis Imperfecta 106
C05.116.099.708.702 Osteosclerosis 38
C05.116.099.708.779 Pycnodysostosis 2
C05.116.099.708.857 Short Rib-Polydactyly Syndrome 3
C05.116.099.708.928 Slipped Capital Femoral Epiphyses 16
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
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 30
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 30
C16.131.831.350.856 Pachyonychia Congenita 3
C16.320 Genetic Diseases, Inborn 1 215
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 30
C16.320.850.250.856 Pachyonychia Congenita 3
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 801
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 30
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 30
C17.800.827.250.856 Pachyonychia Congenita 3

Asphyxiating Thoracic Dystrophy 2 Disease MeSH Browser

Jeune syndrome Disease MeSH Browser

Jeune syndrome situs inversus Disease MeSH Browser

Add