Mondo Disease Ontology
4796 terms(s) returned
| Term Type: | Record: 3701 to 3750 of 4796 Records | Page: 75 of 96, First Previous Next Last | Show Records Per Page |
- spondyloepimetaphyseal dysplasia, Isidor type
- spondyloepimetaphyseal dysplasia, Isidor-Toutain type
- spondyloepimetaphyseal dysplasia, Krakow type
- spondyloepimetaphyseal dysplasia, Li-Shao-Li type
- spondyloepimetaphyseal dysplasia, Maroteaux type
- spondyloepimetaphyseal dysplasia, Missouri type
- spondyloepimetaphyseal dysplasia, PAPSS2 type
- spondyloepimetaphyseal dysplasia, Shohat type
- spondyloepimetaphyseal dysplasia, Strudwick type
- spondyloepimetaphyseal dysplasia, aggrecan type
- spondyloepimetaphyseal dysplasia, di rocco type
- spondyloepimetaphyseal dysplasia, matrilin-3 type
- spondyloepimetaphyseal dysplasia, sponastrime type
- spondyloepimetaphyseal dysplasia-abnormal dentition syndrome
- spondyloepimetaphyseal dysplasia-hypotrichosis syndrome
- spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- spondyloepiphyseal dysplasia
- spondyloepiphyseal dysplasia congenita
- spondyloepiphyseal dysplasia tarda
- spondyloepiphyseal dysplasia tarda with characteristic facies
- spondyloepiphyseal dysplasia tarda, Kohn type
- spondyloepiphyseal dysplasia tarda, X-linked
- spondyloepiphyseal dysplasia tarda, autosomal dominant
- spondyloepiphyseal dysplasia tarda, autosomal recessive
- spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type
- spondyloepiphyseal dysplasia tarda, medaka
- spondyloepiphyseal dysplasia with congenital joint dislocations
- spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability
- spondyloepiphyseal dysplasia with metatarsal shortening
- spondyloepiphyseal dysplasia with punctate corneal dystrophy
- spondyloepiphyseal dysplasia, Cantu type
- spondyloepiphyseal dysplasia, Holling type
- spondyloepiphyseal dysplasia, Kimberley type
- spondyloepiphyseal dysplasia, MacDermot type
- spondyloepiphyseal dysplasia, Reardon type
- spondyloepiphyseal dysplasia, Stanescu type
- spondyloepiphyseal dysplasia, kondo-fu type
- spondyloepiphyseal dysplasia, nishimura type
- spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis
- spondylolisthesis
- spondylolisthesis, chicken
- spondylolisthesis, non-human animal
- spondylolysis
- spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness
- spondylometaphyseal dysplasia
- spondylometaphyseal dysplasia with corneal dystrophy
- spondylometaphyseal dysplasia, 'corner fracture' type
- spondylometaphyseal dysplasia, A4 type
- spondylometaphyseal dysplasia, Czarny-Ratajczak type
- spondylometaphyseal dysplasia, East African type
