Kosmix
One sec... we're building your guide for
Achondrogenesis Type 2
Achondrogenesis type 2
Overview
Anatomy
Main ›
Anatomy ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Congenital disorders
(8)
Achondrogenesis
Achondrogenesis type 1B
Buschke-Ollendorff syndrome
Bethlem myopathy
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Fibrochondrogenesis
Congenital bilateral absence of vas deferens
Congenital malformations
more...
Medical condition
(40)
Hypochondrogenesis
Atelosteogenesis type 2
Ichthyosis bullosa of siemens
Marshall syndrome
Pelger-Huet anomaly
Pelger-Huet anomaly
Diastrophic dysplasia
Anonychia onychodystrophy
Spondyloep- imetaphyseal dysplasia, Strudwick type
Asphyxiating thoracic dystrophy
Alzheimer disease type 2
Raine syndrome
Kniest dysplasia
Multiple epiphyseal dysplasia
Boomerang dysplasia
Epidermolysis bullosa dystrophica
Aceruloplasminemia
Osteochond- rodysplasia
Alport syndrome
Spondyloepiphyseal dysplasia
Antley-bixler syndrome
Dwarfism
Skeletal dysplasias
Stickler syndrome
Pseudoacho- ndroplasia
Hypochondroplasia
Steatocystoma multiplex
Aplasia cutis congenita
Chondromatous
Neurofibromatosis type II
Achondroplasia
Bullous pemphigoid
Dysostosis
Thanatophoric dysplasia
Brachydactyly
Noonan syndrome
Osteogenesis imperfecta
Scoliosis
Bethlem myopathy
Ehlers Danlos Syndrome
Fibrochondrogenesis
more...
Tissues
Keratinopathy
Cartilage
Ossification
Syndromes
(9)
Laminopathy
Barraquer-Simons Syndrome
Buschke-Ollendorff syndrome
Marshall syndrome
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Raine syndrome
Alport syndrome
Stickler syndrome
Noonan syndrome
more...
Genetic disorder
Spondyloperipheral dysplasia
Buschke-Ollendorff syndrome
Aceruloplasminemia
Brachydactyly
Rare diseases
(9)
Atelosteogenesis, type II
Barraquer-Simons Syndrome
Marshall syndrome
Fibrochondrogenesis
Raine syndrome
Raine syndrome
Multiple epiphyseal dysplasia
Boomerang dysplasia
Stickler syndrome
Thanatophoric dysplasia
more...
Autosomal recessive disorders
(8)
Otospondyl- omegaepiphyseal dysplasia
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Very long-chain acyl coenzyme A dehydrogenase deficiency
Atelosteogenesis, type II
Diastrophic dysplasia
Diastrophic dysplasia
Fibrochondrogenesis
Raine syndrome
Aceruloplasminemia
more...
Skeletal system
Metaphyseal
Skeletal disorders
Osseous
Hypochondroplasia
Cartilage
Ossification
See also
(20)
Diseases and disorders
Schmid metaphyseal chondrodysplasia
Scleroprotein
Collagenopathy, types II and XI
COL2A1 gene
COL2A1 gene
SLC26A2
Andersen-Tawil syndrome
Type II collagen
Osteochondropathy
Autoimmune
COL11A1
Short stature
Autosomal dominant
Autosomal recessive
COL11A2
Prenatal diagnosis
FGFR3
Prenatal ultrasound
Short limbs
Differential diagnosis
more...
more categories...
Health Providers & Organizations
›
Vitals.com
