Cleidocranial Dysplasia [kleidokraniální dysplazie]

topical
7
Terms

dysostosis cleidocranialis
kleido-kraniální dysplazie
Scheuthauerův-Marieův-Saintonův syndrom

 

Cleidocranial Digital Dysostosis
Cleidocranial Dysostosis
Dysostosis, Cleidocranial
Marie-Sainton Syndrome
Scheuthauer-Marie-Sainton Syndrome

Persistent link   https://www.medvik.cz/link/D002973
Definition

Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES); wide PUBIC SYMPHYSIS; short middle phalanges of the fifth fingers; and dental and vertebral anomalies.

DUI
D002973 MeSH Browser
CUI
M0004550
History note
85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84
Online note
use CLEIDOCRANIAL DYSPLASIA to search CLEIDOCRANIAL DYSOSTOSIS l966-84
Public note
85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84

C Diseases
C05.116 Bone Diseases 792
C05.116.099.708 Osteochondrodysplasias 123
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 12
C05.116.099.708.375 Fibrous Dysplasia of Bone 47
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
C05.660.207.103 22q11 Deletion Syndrome 2
C05.660.207.207 Cleidocranial Dysplasia 7
C05.660.207.219 Costello Syndrome 3
C05.660.207.231 Craniofacial Dysostosis 28
C05.660.207.240 Craniosynostoses 55
C05.660.207.325 Donohue Syndrome 1
C05.660.207.410 Holoprosencephaly 8
C05.660.207.525 LEOPARD Syndrome 11
C05.660.207.532 Loeys-Dietz Syndrome 7
C05.660.207.536 Megalencephaly 7
C05.660.207.620 Microcephaly 78
C05.660.207.690 Noonan Syndrome 52
C05.660.207.700 Orofaciodigital Syndromes 7
C05.660.207.707 Plagiocephaly 3
C05.660.207.720 Platybasia 12
C05.660.207.850 Rubinstein-Taybi Syndrome 12
C05.660.207.925 Silver-Russell Syndrome 3
C16.131.621.207 Craniofacial Abnormalities 77
C16.131.621.207.103 22q11 Deletion Syndrome 2
C16.131.621.207.207 Cleidocranial Dysplasia 7
C16.131.621.207.231 Craniofacial Dysostosis 28
C16.131.621.207.240 Craniosynostoses 55
C16.131.621.207.410 Holoprosencephaly 8
C16.131.621.207.525 LEOPARD Syndrome 11
C16.131.621.207.532 Megalencephaly 7
C16.131.621.207.540 Maxillofacial Abnormalities 28
C16.131.621.207.620 Microcephaly 78
C16.131.621.207.690 Noonan Syndrome 52
C16.131.621.207.700 Orofaciodigital Syndromes 7
C16.131.621.207.707 Plagiocephaly 3
C16.131.621.207.720 Platybasia 12
C16.131.621.207.850 Rubinstein-Taybi Syndrome 12

Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only Disease MeSH Browser

Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly Disease MeSH Browser

Cleidocranial Dysplasia, Recessive Form Disease MeSH Browser

Parietal Foramina With Cleidocranial Dysplasia Disease MeSH Browser

Yunis Varon syndrome Disease MeSH Browser