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 224 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
- Camurati–Engelmann disease
- Carpenter–Hunter type
- Cataract skeletal anomalies
- Catel–Manzke syndrome
- Caudal regression sequence
- Chondrodysplasia Blomstrand
- Chondrodysplasia lethal recessive
- Chondrodysplasia pseudohermaphrodism syndrome
- Chondrodysplasia punctata
- Chondrodysplasia punctata with steroid sulfatase deficiency
- Chondrodysplasia, Grebe type
- Chondrodystrophy
- Chondrysplasia punctata, humero-metacarpal type
- Chronic recurrent multifocal osteomyelitis
- Cleidocranial dysplasia micrognathia absent thumbs
- Cloverleaf skull bone dysplasia
- Cloverleaf skull micromelia thoracic dysplasia
- Coloboma of macula-brachydactyly type B syndrome
- Congenital skeletal disorder
- Cortical hyperostosis syndactyly
- Craniofaciocervical osteoglyphic dysplasia
- Craniomicromelic syndrome
- Cushing's symphalangism
D
- Deafness skeletal dysplasia lip granuloma
- Deafness symphalangism
- Dermatocardioskeletal syndrome Boronne type
- Diastrophic dwarf
- Diastrophic dysplasia
- 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
- 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
- Maroteaux–Verloes–Stanescu 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
R
- Radioulnar synostosis mental retardation hypotonia
- Ramer–Ladda syndrome
- Recessive multiple epiphyseal dysplasia
- Reginato–Shiapachasse syndrome
- Reinhardt–Pfeiffer syndrome
- Rhizomelia
- Rhizomelic dysplasia type Patterson–Lowry
- Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
- Rickets
- Robinow syndrome
- Rudiger syndrome
S
- Scapuloiliac dysostosis
- Schmitt Gillenwater Kelly syndrome
- Schneckenbecken dysplasia
- Schwartz sign
- Schwartz Jampel syndrome
- Schwartz–lelek syndrome
- Sclerosing bone dysplasia mental retardation
- Severe achondroplasia with developmental delay and acanthosis nigricans
- Short stature dysmorphic face pelvic scapula dysplasia
- Short-limb skeletal dysplasia with severe combined immunodeficiency
- Skeletal dysplasia epilepsy short stature
- Skeletal dysplasia orofacial anomalies
- Skeletal dysplasia San diego type
- Skeleto cardiac syndrome with thrombocytopenia
- Slipped capital femoral epiphysis
- 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
- Spondylometaphyseal dysplasia, 'corner fracture' t
- Spondylometaphyseal dysplasia, Schmidt type
- Spondylometaphyseal dysplasia, Sedaghatian type
- Spondylometaphyseal dysplasia, X-linked
