Short Rib-Polydactyly Syndrome [syndrom krátkého žebra a polydaktylie]

topical
3
Terms

Majewski syndrom
Majewskiho syndrom
Saldino-Noonan syndrom
Saldino-Noonanův syndrom
syndrom krátkého žebra a polydaktylie typ I
syndrom krátkého žebra a polydaktylie typ II
syndrom krátkého žebra a polydaktylie, typ Majewski
syndrom krátkého žebra a polydaktylie, typ Saldino-Noonan

 

Asphyxiating Thoracic Dystrophy 3
Majewski Syndrome
Polydactyly with Neonatal Chondrodystrophy, Type 1
Polydactyly with Neonatal Chondrodystrophy, Type 2
Polydactyly With Neonatal Chondrodystrophy, Type I
Polydactyly With Neonatal Chondrodystrophy, Type II
Saldino-Noonan Syndrome
Short Rib-Polydactyly Syndrome Type 1
Short Rib-Polydactyly Syndrome, Majewski Type
Short Rib-Polydactyly Syndrome, Saldino-Noonan Type
Short Rib-Polydactyly Syndrome, Type I
Short Rib-Polydactyly Syndrome, Type II

Persistent link   https://www.medvik.cz/link/D012779
Definition

A syndrome inherited as an autosomal recessive trait and incompatible with life. The main features are narrow thorax, short ribs, scapular and pelvic dysplasia, and polydactyly.

Annotation
do not confuse entry term SALDINO-NOONAN SYNDROME with NOONAN SYNDROME
DUI
D012779 MeSH Browser
CUI
M0019797
Previous indexing
Abnormalities, Multiple (1968-1984); Fingers (1966-1984); Ribs (1966-1984)
History note
1991(1985);use OSTEOCHONDRODYSPLASIAS 1985-1990
Public note
1991; see OSTEOCHONDRODYSPLASIAS 1985-1990

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced 1
CL
classification
CO
complications
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 2
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
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 1 123
C05.116 Bone Diseases 796
C05.116.099 Bone Diseases, Developmental 292
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
C05.660 Musculoskeletal Abnormalities 107
C05.660.585 Limb Deformities, Congenital 126
C05.660.585.600 Polydactyly 31
C05.660.585.600.374 Pallister-Hall Syndrome
C05.660.585.600.750 Short Rib-Polydactyly Syndrome 3
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 749
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
C16.131.077.371 Fraser Syndrome 2
C16.131.077.393 Gardner Syndrome 21
C16.131.077.401 Heterotaxy Syndrome 7
C16.131.077.410 Holoprosencephaly 8
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
C16.131.621 Musculoskeletal Abnormalities 107
C16.131.621.585 Limb Deformities, Congenital 126
C16.131.621.585.600 Polydactyly 31
C16.131.621.585.600.374 Pallister-Hall Syndrome
C16.131.621.585.600.750 Short Rib-Polydactyly Syndrome 3

Short rib-polydactyly syndrome, Beemer type Disease MeSH Browser

Short rib-polydactyly syndrome, Verma-Naumoff type Disease MeSH Browser

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