Category:Skeletal disorders
From WikiMD.com Medical Encyclopedia
This category contains disorders of the skeletal system
Subcategories
This category has the following 3 subcategories, out of 3 total.
Pages in category "Skeletal disorders"
The following 200 pages are in this category, out of 216 total.
(previous page) (next page)A
- Accessory navicular bone
- Achondrogenesis type 1B
- Achondrogenesis type 2
- Achondrogenesis type II
- Acromesomelic dysplasia
- Acropectorovertebral dysplasia
- Angel-shaped phalango-epiphyseal dysplasia
- Arthritis
- Atelosteogenesis type I
- Atelosteogenesis, type II
- Autosomal recessive multiple epiphyseal dysplasia
B
C
- Campomelic dysplasia, mild
- Camptodactyly joint contractures facial skeletal dysplasia
- Camurati–Engelmann disease
- Carnevale–Krajewska–Fischetto syndrome
- Carpenter–Hunter type
- Cartilage–hair hypoplasia
- Cassia–Stocco–Dos Santos syndrome
- Cataract skeletal anomalies
- Catel–Manzke syndrome
- Caudal regression sequence
- Cephaloskeletal dysplasia
- Cheney syndrome
- Chitayat–Meunier–Hodgkinson syndrome
- Chondrodysplasia pseudohermaphrodism syndrome
- Chondrodysplasia punctata
- Chondrodysplasia punctata 1, x-linked recessive
- Chondrodysplasia punctata, brachytelephalangic
- Chondrodysplasia, Grebe type
- Chondrodystrophy
- Chondroectodermal dysplasia
- Chromosome 18q deletion syndrome
- Chronic recurrent multifocal osteomyelitis
- Cloverleaf skull bone dysplasia
- Colavita–Kozlowski syndrome
- Coloboma of macula-brachydactyly type B syndrome
- Congenital skeletal disorder
- Conradi Hunermann syndrome
- Corsello–Opitz syndrome
- Cortada–Koussef–Matsumoto syndrome
- Cote–Katsantoni syndrome
- Craniofaciocervical osteoglyphic dysplasia
- Craniomicromelic syndrome
- Craniosynostosis radial aplasia syndrome
- Cushing's symphalangism
- Cutler Bass Romshe syndrome
- Czeizel–Losonci syndrome
D
- Deafness symphalangism
- Dennis–Fairhurst–Moore syndrome
- Dermatocardioskeletal syndrome Boronne type
- Desbuquois Syndrome
- Diastrophic dysplasia
- Drachtman–Weinblatt–Sitarz syndrome
- Du Bois sign
- Duker–Weiss–Siber syndrome
- Dupont–Sellier–Chochillon syndrome
- Dwarfism syndesmodysplasic
- Dyggve–Melchior–Clausen syndrome
- Dysostosis Stanescu type
- Dyssegmental dysplasia glaucoma
E
F
H
- Heart-hand syndrome, Slovenian type
- Hecht Scott syndrome
- Hereditary multiple osteochondromas
- Holzgreve–Wagner–Rehder syndrome
- Hordnes–Engebretsen–Knudtson syndrome
- Houlston–Ironton–Temple syndrome
- Hunter–Carpenter–Mcdonald syndrome
- Hunter–Macpherson syndrome
- Hutteroth–Spranger syndrome
- Hydrocephalus growth retardation skeletal anomalies
- Hydrocephalus skeletal anomalies
- Hypermobility (joints)
- Hypochondrogenesis
J
K
L
M
- Maffucci syndrome
- Maroteaux Stanescu Cousin syndrome
- Maroteaux–Stanescu–Cousin syndrome
- Marshall–White syndrome
- Mega-epiphyseal dwarfism
- Megaepiphyseal dwarfism
- Melorheostosis
- Mesomelia synostoses
- Mesomelic dysplasia Thai type
- Mesomelic syndrome Pfeiffer type
- Metachondromatosis
- Metaphyseal anadysplasia
O
- Ollier disease
- Ollier's disease
- Omodysplasia 2
- Opsismodysplasia
- Osmed syndrome
- Osteoarthritis
- Template:Osteochondrodysplasia
- Osteocraniostenosis
- Osteodystrophy
- Osteofibrous dysplasia
- Osteogenesis imperfecta type II
- Osteogenesis imperfecta type III
- Osteogenesis imperfecta type V
- Osteogenesis imperfecta type VI
- Osteophyte
- Osteoporosis
- Otopalatodigital syndrome type 2
P
- Pacman dysplasia
- Patella hypoplasia mental retardation
- Pelvic shoulder dysplasia
- Peripheral dysostosis
- Platyspondylic lethal skeletal dysplasia Torrance type
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Platyspondyly
- Pseudoachondroplastic dysplasia
- Pseudohermaphroditism female skeletal anomalies
- Pyknoachondrogenesis
R
S
- Sacral agenesis
- Scapuloiliac dysostosis
- Schmitt Gillenwater Kelly syndrome
- Schneckenbecken dysplasia
- Schwartz sign
- Schwartz Jampel syndrome
- Schwartz–lelek syndrome
- Severe achondroplasia with developmental delay and acanthosis nigricans
- Short rib – polydactyly syndrome
- Short rib-polydactyly syndrome, Beermer type
- Short rib-polydactyly syndrome, Saldino-Noonan type
- Short rib-polydactyly syndrome, Verma-Naumoff type
- Short rib–polydactyly syndrome
- Short-limb skeletal dysplasia with severe combined immunodeficiency
- Skeletal dysplasia epilepsy short stature
- Skeletal dysplasia orofacial anomalies
- Sohval–Soffer syndrome
- Spherophakia brachymorphia syndrome
- Spinal dysostosis type Anhalt
- Sponastrime dysplasia
- Spondylo-meta-epiphyseal dysplasia
- Spondylocostal dysostosis
- Spondylocostal dysplasia dominant
- Spondyloepimetaphyseal dysplasia
- Spondyloepimetaphyseal dysplasia Strudwick type
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloepiphyseal dysplasia, congenital type
- Spondylometaphyseal dysplasia with cone-rod dystrophy
- Spondyloperipheral dysplasia
- Spondylosis
