Osteochondrodysplasias [osteochondrodysplazie]

topical
125
Terms

chondrodysplazie
chondrodystrofická myotonie
dyschondroplazie
generalizovaná kortikální hyperostóza
Kniestova dysplazie
Melnick-Needlesův syndrom
Melnickův-Needlesův syndrom
mnohočetná epifyzární dysplazie
myotonická chondrodystrofie
osteochondrodysplázie
osteodysplastie Melnick-Needles
Schwartz-Jampel syndrom
Schwartz-Jampelův syndrom
Schwartz-Jampelův syndrom I. typu
Schwartzův-Jampelův syndrom
Schwartzův-Jampelův syndrom I. typu
spondyloepifyzární dysplazie
spondyloepifyzární dysplazie tarda
van Buchemova nemoc
van Buchemův syndrom

 

Chondrodystrophic Myotonia
Dyschondroplasia
Dyschondroplasias
Endosteal Hyperostosis, Autosomal Recessive
Hyperostosis Corticalis Generalisata
Hyperphosphatasemia Tarda
Late-Onset Spondyloepiphyseal Dysplasia
Melnick-Needles Osteodysplasty
Melnick-Needles Syndrome
Multiple Epiphyseal Dysplasia
Myotonic Chondrodystrophy
Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities
Osteodysplasty of Melnick and Needles
Schwartz Jampel Aberfeld syndrome
Schwartz-Jampel Syndrome
Schwartz-Jampel Syndrome, Type 1
Schwartz-Jampel-Aberfeld Syndrome
SED Tarda
SJA Syndrome
Sost Sclerosing Bone Dysplasia
Sost-Related Sclerosing Bone Dysplasia
Spondylo-Epimetaphyseal Dysplasia With Myotonia
Spondyloepiphyseal Dysplasia
Spondyloepiphyseal Dysplasia Tarda, X-Linked
Spondyloepiphyseal Dysplasia, Late
Van Buchem Disease
X-Linked SED
X-Linked SEDT
X-Linked Spondyloepiphyseal Dysplasia Tarda

Persistent link   https://www.medvik.cz/link/D010009
Definition

Abnormal development of cartilage and bone.

DUI
D010009 MeSH Browser
CUI
M0015525
Previous indexing
Bone Diseases (1966-1969); Bone Diseases, Developmental (1970-1984)
History note
85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLOEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79
Online note
use OSTECHONDRODYSPLASIAS to search DYSCHONDROPLASIAS 1966-84; use MUCOPOLYSACCHARIDOSIS 4 to search SPONDYLOEPIPHYSEAL DYSPLASIA 1968-84
Public note
85; DYSCHONDRODYSPLASIAS was heading DYSCHONDROPLASIA 1963-84; SPONDYLEPIPHYSEAL DYSPLASIA was see MUCOPOLYSACCHARIDOSIS 4 1980-84, was see ECCENTROOSTEOCHONDRODYSPLASIA 1968-79

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 20
CO
complications 6
CN
congenital 3
DI
diagnosis 36
DG
diagnostic imaging 5
DH
diet therapy
DT
drug therapy 4
EC
economics
EM
embryology 1
EN
enzymology
EP
epidemiology 2
EH
ethnology
ET
etiology 14
GE
genetics 35
HI
history 1
IM
immunology 3
ME
metabolism 2
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 12
PP
physiopathology 3
PC
prevention & control 2
PX
psychology
RT
radiotherapy
RH
rehabilitation 3
SU
surgery 10
TH
therapy 20
UR
urine
VE
veterinary
VI
virology

C Diseases
C05 Musculoskeletal Diseases 1 136
C05.116 Bone Diseases 796
C05.116.099 Bone Diseases, Developmental 294
C05.116.099.052 Acro-Osteolysis 3
C05.116.099.105 Basal Cell Nevus Syndrome 33
C05.116.099.343 Dwarfism 99
C05.116.099.370 Dysostoses 22
C05.116.099.386 Funnel Chest 39
C05.116.099.492 Gigantism 14
C05.116.099.655 Leg Length Inequality 119
C05.116.099.674 Marfan Syndrome 105
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
C05.116.099.736 Osteolysis, Essential 8
C05.116.099.739 Pectus Carinatum 1
C05.116.099.742 Platybasia 12
C05.116.099.750 Proteus Syndrome 8
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 219
C16.320.033 Adrenal Hyperplasia, Congenital 227
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 88
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
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 261
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 335
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 61
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 61
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 48
C16.320.400 Heredodegenerative Disorders, Nervous System 47
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 7
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 715
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 149
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 51
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 91
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Achondrogenesis Disease MeSH Browser

Acrodysostosis Disease MeSH Browser

Acrodysplasia scoliosis Disease MeSH Browser

Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia Disease MeSH Browser

Acromesomelic dysplasia Disease MeSH Browser

Acromesomelic dysplasia Campailla-Martinelli type Disease MeSH Browser

Acropectorovertebral Dysplasia, F-Form Disease MeSH Browser

Akaba Hayasaka syndrome Disease MeSH Browser

Anauxetic dysplasia Disease MeSH Browser

Atelosteogenesis Type 3 Disease MeSH Browser

Atelosteogenesis type 2 Disease MeSH Browser

Atelosteogenesis, type 1 Disease MeSH Browser

Auriculoosteodysplasia Disease MeSH Browser

Boomerang dysplasia Disease MeSH Browser

Brachyolmia Disease MeSH Browser

Brachyolmia Type 2 Disease MeSH Browser

Brachyolmia Type 3 Disease MeSH Browser

Brachyolmia, recessive Hobaek type Disease MeSH Browser

CODAS syndrome Disease MeSH Browser

Cantu syndrome Disease MeSH Browser

Chondrodysplasia Calcificans Metaphysealis Disease MeSH Browser

Chondrodysplasia, Grebe type Disease MeSH Browser

Chondrodysplasia, Lethal, with Long Bone Angulation and Mixed Bone Density Disease MeSH Browser

Chondrodysplasia, Megarbane-Dagher-Melki Type Disease MeSH Browser

Chondrodysplasia, blomstrand type Disease MeSH Browser

Cleidorhizomelic syndrome Disease MeSH Browser

Cloverleaf skull micromelia thoracic dysplasia Disease MeSH Browser

Collagenopathy, type 2 alpha 1 Disease MeSH Browser

Coloboma of Alar-nasal cartilages with telecanthus Disease MeSH Browser

Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia Disease MeSH Browser

Craniodiaphyseal Dysplasia Disease MeSH Browser

Craniodiaphyseal Dysplasia, Autosomal Dominant Disease MeSH Browser

Czech dysplasia, metatarsal type Disease MeSH Browser

Dyschondrosteosis and Nephritis Disease MeSH Browser

Eiken Skeletal Dysplasia Disease MeSH Browser

Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness Disease MeSH Browser

Epiphyseal Dysplasia, Baumann Type Disease MeSH Browser

Epiphyseal Dysplasia, Multiple, with Miniepiphyses Disease MeSH Browser

Epiphyseal Dysplasia, Multiple, with Myopathy Disease MeSH Browser

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Disease MeSH Browser

Epiphyseal Dysplasia, Multiple, with Severe Proximal Femoral Dysplasia Disease MeSH Browser

Epiphyseal dysplasia, multiple, 1 Disease MeSH Browser

Epiphyseal dysplasia, multiple, 2 Disease MeSH Browser

Epiphyseal dysplasia, multiple, 3 Disease MeSH Browser

Epiphyseal dysplasia, multiple, 4 Disease MeSH Browser

Epiphyseal dysplasia, multiple, 5 Disease MeSH Browser

Fairbank disease Disease MeSH Browser

Faye-Petersen Ward Carey syndrome Disease MeSH Browser

Fraser Jequier Chen syndrome Disease MeSH Browser

Frontometaphyseal dysplasia Disease MeSH Browser

Frontootopalatodigital Osteodysplasia Disease MeSH Browser

Ghosal Hematodiaphyseal Dysplasia Disease MeSH Browser

HEM dysplasia Disease MeSH Browser

Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia Disease MeSH Browser

Hip Dysplasia, Beukes Type Disease MeSH Browser

Hypochondrogenesis Disease MeSH Browser

Hypoparathyroidism-retardation-dysmorphism syndrome Disease MeSH Browser

Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies Disease MeSH Browser

Jansen type metaphyseal chondrodysplasia Disease MeSH Browser

Jequier Kozlowski skeletal dysplasia Disease MeSH Browser

Kniest dysplasia Disease MeSH Browser

Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis Disease MeSH Browser

Kozlowski Tsuruta Taki syndrome Disease MeSH Browser

Langer mesomelic dysplasia Disease MeSH Browser

Laplane Fontaine Lagardere syndrome Disease MeSH Browser

Larsen Syndrome Disease MeSH Browser

Larsen syndrome, dominant type Disease MeSH Browser

Larsen-Like Syndrome Disease MeSH Browser

Leri-Weil syndrome Disease MeSH Browser

Lowry Wood syndrome Disease MeSH Browser

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Disease MeSH Browser

Madelung Deformity Disease MeSH Browser

Marshall syndrome Disease MeSH Browser

Megaepiphyseal dwarfism Disease MeSH Browser

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Disease MeSH Browser

Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type Disease MeSH Browser

Mesomelic Dysplasia, Savarirayan Type Disease MeSH Browser

Mesomelic dwarfism Reinhardt Pfeiffer type Disease MeSH Browser

Metaphyseal Anadysplasia 1 Disease MeSH Browser

Metaphyseal Anadysplasia 2 Disease MeSH Browser

Metaphyseal Chondrodysplasia with Retinitis Pigmentosa Disease MeSH Browser

Metaphyseal Chondrodysplasia, Kaitila Type Disease MeSH Browser

Metaphyseal Chondrodysplasia, Pena Type Disease MeSH Browser

Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly Disease MeSH Browser

Metaphyseal Dysplasia without Hypotrichosis Disease MeSH Browser

Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy Disease MeSH Browser

Metaphyseal Dysplasia, Braun-Tinschert Type Disease MeSH Browser

Metaphyseal anadysplasia Disease MeSH Browser

Metaphyseal chondrodysplasia Schmid type Disease MeSH Browser

Metaphyseal chondrodysplasia Spahr type Disease MeSH Browser

Metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands Disease MeSH Browser

Metaphyseal undermodeling, spondylar dysplasia, and overgrowth Disease MeSH Browser

Metatropic Dwarfism, Type II Disease MeSH Browser

Metatropic dwarfism Disease MeSH Browser

Microcephalic Osteodysplastic Primordial Dwarfism, Type II Disease MeSH Browser

Microcephalic osteodysplastic primordial dwarfism, type 1 Disease MeSH Browser

Microcephaly-Micromelia Syndrome Disease MeSH Browser

Micromelic dwarfism Fryns type Disease MeSH Browser

Micromelic dysplasia, congenital, with dislocation of radius Disease MeSH Browser

Multiple Congenital Anomalies Syndrome with Cloverleaf Skull Disease MeSH Browser

Multiple Epiphyseal Dysplasia with Robin Phenotype Disease MeSH Browser

Nievergelt syndrome Disease MeSH Browser

Nivelon Nivelon Mabille syndrome Disease MeSH Browser

Omodysplasia 2 Disease MeSH Browser

Opsismodysplasia Disease MeSH Browser

Osebold Skeletal Dysplasia Osteolysis Syndrome Disease MeSH Browser

Osteoarthritis with Mild Chondrodysplasia Disease MeSH Browser

Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension Disease MeSH Browser

Osteodysplasia, Familial, Anderson Type Disease MeSH Browser

Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski Disease MeSH Browser

Osteoglophonic dwarfism Disease MeSH Browser

Oto-Palato-digital syndrome type 1 Disease MeSH Browser

Oto-palato-digital syndrome, type 2 Disease MeSH Browser

Otopalatodigital Spectrum Disorder Disease MeSH Browser

Pelvis-Shoulder Dysplasia Disease MeSH Browser

Pierre Robin syndrome with fetal chondrodysplasia Disease MeSH Browser

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Disease MeSH Browser

Polydysspondyly Disease MeSH Browser

Pubic Bone Dysplasia Disease MeSH Browser

Pyle disease Disease MeSH Browser

Roifman syndrome Disease MeSH Browser

Schaefer Stein Oshman syndrome Disease MeSH Browser

Schimke immunoosseous dysplasia Disease MeSH Browser

Schneckenbecken dysplasia Disease MeSH Browser

Short stature syndrome, Brussels type Disease MeSH Browser

Situs inversus totalis with cystic dysplasia of kidneys and pancreas Disease MeSH Browser

Skeletal dysplasia coarse facies mental retardation Disease MeSH Browser

Smith-McCort Dysplasia Disease MeSH Browser

Spinal Dysplasia, Anhalt Type Disease MeSH Browser

Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Disease MeSH Browser

Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like Disease MeSH Browser

Spondylodysplasia And Premature Pubarche Disease MeSH Browser

Spondyloenchondrodysplasia Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia With Abnormal Dentition Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia With Joint Laxity Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, Irapa Type Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, Missouri Type Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, Pakistani Type Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, Shohat Type Disease MeSH Browser

Spondyloepimetaphyseal Dysplasia, X-Linked Disease MeSH Browser

Spondyloepimetaphyseal dysplasia with hypotrichosis Disease MeSH Browser

Spondyloepimetaphyseal dysplasia with multiple dislocations Disease MeSH Browser

Spondyloepimetaphyseal dysplasia, Genevieve type Disease MeSH Browser

Spondyloepimetaphyseal dysplasia, sponastrime type Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda with Mental Retardation Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive Disease MeSH Browser

Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type Disease MeSH Browser

Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation Disease MeSH Browser

Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy Disease MeSH Browser

Spondyloepiphyseal Dysplasia with Atlantoaxial Instability Disease MeSH Browser

Spondyloepiphyseal Dysplasia, Kimberley Type Disease MeSH Browser

Spondyloepiphyseal Dysplasia, Myopia, And Sensorineural Deafness Disease MeSH Browser

Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech Disease MeSH Browser

Spondyloepiphyseal dysplasia tarda, Toledo type Disease MeSH Browser

Spondyloepiphyseal dysplasia, Omani type Disease MeSH Browser

Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness Disease MeSH Browser

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Disease MeSH Browser

Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy Disease MeSH Browser

Spondylometaphyseal Dysplasia, Type A4 Disease MeSH Browser

Spondylometaphyseal Dysplasia, X-Linked Disease MeSH Browser

Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism Disease MeSH Browser

Spondylometaphyseal dysplasia with dentinogenesis imperfecta Disease MeSH Browser

Spondylometaphyseal dysplasia, 'corner fracture' type Disease MeSH Browser

Spondylometaphyseal dysplasia, Algerian type Disease MeSH Browser

Spondylometaphyseal dysplasia, Kozlowski type Disease MeSH Browser

Spondylometaphyseal dysplasia, Sedaghatian type Disease MeSH Browser

Spondylometaphyseal dysplasia, axial Disease MeSH Browser

Spondylometaphyseal dysplasia, east-African type Disease MeSH Browser

Spondyloocular Syndrome, Autosomal Recessive Disease MeSH Browser

Spondyloperipheral dysplasia short ulna Disease MeSH Browser

Spondylospinal Thoracic Dysostosis Disease MeSH Browser

Strudwick syndrome Disease MeSH Browser

Stuve-Wiedemann syndrome Disease MeSH Browser

Teebi Naguib Al Awadi syndrome Disease MeSH Browser

Terminal Osseous Dysplasia and Pigmentary Defects Disease MeSH Browser

Thoracolaryngopelvic dysplasia Disease MeSH Browser

Tracheobronchopathia osteoplastica Disease MeSH Browser

Trichoscyphodysplasia Disease MeSH Browser

Ulna metaphyseal dysplasia syndrome Disease MeSH Browser

Upington disease Disease MeSH Browser

Van Buchem disease type 2 Disease MeSH Browser

Verloes Bourguignon syndrome Disease MeSH Browser

Verloes Van Maldergem Marneffe syndrome Disease MeSH Browser

Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia Disease MeSH Browser

Wolcott-Rallison syndrome Disease MeSH Browser

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