Experimental Factor Ontology
133 terms(s) returned
Term Type: | Record: 51 to 100 of 133 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- Spastic paraparesis - deafness
- Spastic paraplegia - Paget disease of bone
- Spastic paraplegia - epilepsy - intellectual disability
- Spastic paraplegia - facial-cutaneous lesions
- Spastic paraplegia - glaucoma - intellectual disability
- Spastic paraplegia - nephritis - deafness
- Spastic paraplegia - neuropathy - poikiloderma
- Spastic paraplegia - precocious puberty
- Spastic paraplegia type 2
- Spastic paraplegia-optic atrophy-neuropathy syndrome
- Spastic tetraplegia - retinitis pigmentosa - intellectual disability
- Spasticity - intellectual disability - X-linked epilepsy
- Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells
- Spectrin-associated autosomal recessive cerebellar ataxia
- Spina bifida - hypospadias
- Spinal atrophy - ophthalmoplegia - pyramidal syndrome
- Spinal muscular atrophy - Dandy-Walker malformation - cataracts
- Spinal muscular atrophy associated with central nervous system anomaly
- Spinal muscular atrophy with respiratory distress type 1
- Spinocerebellar ataxia - dysmorphism
- Spinocerebellar ataxia type 1 with axonal neuropathy
- Spinocerebellar ataxia type 3
- Spinocerebellar ataxia with axonal neuropathy type 2
- Spinocerebellar ataxia with oculomotor anomaly
- Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly
- Splenogonadal fusion - limb defects - micrognathia
- Split hand - split foot - deafness
- Split hand - urinary anomalies - spina bifida
- Split hand-split foot malformation
- Spondylocarpotarsal synostosis
- Spondylocostal dysostosis - anal and genitourinary malformations
- Spondylocostal dysostosis - hypospadias - intellectual disability
- Spondyloepimetaphyseal dysplasia - abnormal dentition
- Spondyloepimetaphyseal dysplasia - hypotrichosis
- Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification
- Spondyloepimetaphyseal dysplasia congenita, Strudwick type
- Spondyloepimetaphyseal dysplasia, Pakistani type
- Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia
- Spondyloepiphyseal dysplasia, Maroteaux type
- Spondyloepiphyseal dysplasia, Nishimura type
- Spondylometaphyseal dysplasia - bowed forearms - facial dysmorphism
- Spondylometaphyseal dysplasia - cone-rod dystrophy
- Spondyloperipheral dysplasia - short ulna
- Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
- Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
- Steatocystoma multiplex - natal teeth
- Steinert myotonic dystrophy
- Steroid dehydrogenase deficiency - dental anomalies
- Stickler syndrome type 3
- Stormorken-Sjaastad-Langslet syndrome