Category:Skeletal disorders
From WikiMD's Wellness Encyclopedia
This category contains disorders of the skeletal system
Subcategories
This category has the following 2 subcategories, out of 2 total.
Pages in category "Skeletal disorders"
The following 200 pages are in this category, out of 263 total.
(previous page) (next page)A
B
- Barrel chest
- Blomstrand syndrome
- Blount disease
- Bone dysplasia Azouz type
- Bone dysplasia corpus callosum agenesis
- Bone dysplasia Moore type
- Bow legs
- Bowed legs
- Brachydactyly preaxial hallux varus
- Brachydactyly tibial hypoplasia
- Brachydactyly-elbow wrist dysplasia syndrome
- Brachymesomelia renal syndrome
- Brachymesophalangy type 2
- Brachyolmia
- Bruck syndrome
- Bruck syndrome 1
C
- Camptodactyly joint contractures facial skeletal dysplasia
- Camurati–Engelmann disease
- Carnevale–Krajewska–Fischetto syndrome
- Carpenter–Hunter type
- Cassia–Stocco–Dos Santos syndrome
- Cataract skeletal anomalies
- Catel–Manzke syndrome
- Caudal regression sequence
- Chitayat–Meunier–Hodgkinson syndrome
- Chondrodysplasia Blomstrand
- Chondrodysplasia lethal recessive
- Chondrodysplasia pseudohermaphrodism syndrome
- Chondrodysplasia punctata
- Chondrodysplasia punctata 1, x-linked recessive
- Chondrodysplasia punctata with steroid sulfatase deficiency
- Chondrodysplasia punctata, brachytelephalangic
- Chondrodysplasia, Grebe type
- Chondrodystrophy
- Chondroectodermal dysplasia
- Chondrysplasia punctata, humero-metacarpal type
- Chromosome 18q deletion syndrome
- Chronic recurrent multifocal osteomyelitis
- Cleidocranial dysplasia micrognathia absent thumbs
- Cloverleaf skull bone dysplasia
- Cloverleaf skull micromelia thoracic dysplasia
- Colavita–Kozlowski syndrome
- Coloboma of macula-brachydactyly type B syndrome
- Congenital skeletal disorder
- Corsello–Opitz syndrome
- Cortada–Koussef–Matsumoto syndrome
- Cortical hyperostosis syndactyly
- Cote–Katsantoni syndrome
- Craniofaciocervical osteoglyphic dysplasia
- Craniomicromelic syndrome
- Craniosynostosis radial aplasia syndrome
- Cushing's symphalangism
- Cutler Bass Romshe syndrome
- Czeizel–Losonci syndrome
D
- Deafness skeletal dysplasia lip granuloma
- Deafness symphalangism
- Dennis–Fairhurst–Moore syndrome
- Dermatocardioskeletal syndrome Boronne type
- Desbuquois Syndrome
- Diastrophic dwarf
- Diastrophic dysplasia
- Drachtman–Weinblatt–Sitarz syndrome
- Duker–Weiss–Siber syndrome
- Dupont–Sellier–Chochillon syndrome
- Dwarfism syndesmodysplasic
- Dyggve–Melchior–Clausen syndrome
- Dysostosis acral with facial and genital abnormalities
- Dysostosis Stanescu type
- Dyssegmental dysplasia glaucoma
- Dyssegmental dysplasia Silverman–Handmaker type
E
F
H
- Heart-hand syndrome, Slovenian type
- Hecht Scott syndrome
- Hereditary multiple osteochondromas
- Hirsutism skeletal dysplasia mental retardation
- Holzgreve–Wagner–Rehder syndrome
- Hordnes–Engebretsen–Knudtson syndrome
- Houlston–Ironton–Temple syndrome
- Hunter–Carpenter–Mcdonald syndrome
- Hunter–Macpherson syndrome
- Hutteroth–Spranger syndrome
- Hydrocephalus costovertebral dysplasia Sprengel anomaly
- Hydrocephalus growth retardation skeletal anomalies
- Hydrocephalus skeletal anomalies
- Hypermobility (joints)
- Hypochondrogenesis
- Hypoplasia of the tibia with polydactyly
J
K
L
M
- Macroepiphyseal dysplasia Mcalister Coe type
- Maroteaux–Stanescu–Cousin syndrome
- Marshall–White syndrome
- MASS syndrome
- Mega-epiphyseal dwarfism
- Melorheostosis
- Mesomelia synostoses
- Mesomelic dwarfism Reinhardt–Pfeiffer type
- Mesomelic dysplasia skin dimples
- Mesomelic dysplasia Thai type
- Mesomelic syndrome Pfeiffer type
- Metachondromatosis
- Metaphyseal anadysplasia
- Metaphyseal chondrodysplasia, others
- Metaphyseal dysplasia Pyle type
- Micromelic dysplasia dislocation of radius
- Mitral regurgitation deafness skeletal anomalies
- Multiple joint dislocations metaphyseal dysplasia
O
- Ollier disease
- Ollier's disease
- Opsismodysplasia
- Osmed syndrome
- Osteoarthritis
- Template:Osteochondrodysplasia
- Osteochondrodysplasia thrombocytopenia hydrocephalus
- 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
- Platyspondylic lethal chondrodysplasia
- Platyspondylic lethal skeletal dysplasia
- Platyspondylic lethal skeletal dysplasia Torrance type
- Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Platyspondyly
- Pseudoachondroplastic dysplasia
- Pseudoachondroplastic dysplasia 1
- Pseudohermaphroditism female skeletal anomalies
- Pyknoachondrogenesis
