Mondo Disease Ontology
4158 terms(s) returned
| Term Type: | Record: 3201 to 3250 of 4158 Records | Page: 65 of 84, First Previous Next Last | Show Records Per Page |
- spondylocostal dysostosis 4, autosomal recessive
- spondylocostal dysostosis 5
- spondylocostal dysostosis 6, autosomal recessive
- spondylocostal dysostosis, autosomal recessive, dog
- spondylocostal dysostosis, autosomal recessive, non-human animal
- spondylocostal dysostosis-anal and genitourinary malformations syndrome
- spondylocostal dysostosis-hypospadias-intellectual disability syndrome
- spondylodysplastic Ehlers-Danlos syndrome
- spondylodysplastic dysplasia
- spondyloepimetaphyseal dysplasia
- spondyloepimetaphyseal dysplasia with joint laxity
- spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
- spondyloepimetaphyseal dysplasia with joint laxity, type 3
- spondyloepimetaphyseal dysplasia with multiple dislocations
- spondyloepimetaphyseal dysplasia, Bieganski type
- spondyloepimetaphyseal dysplasia, Genevieve type
- spondyloepimetaphyseal dysplasia, Guo-Campeau type
- spondyloepimetaphyseal dysplasia, Handigodu type
- spondyloepimetaphyseal dysplasia, Irapa type
- 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 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, Kimberley type
