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Genetic Conditions…
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© 2006 Betterchem Corp.
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[Index] | [Continue]
- Sack-Barabas syndrome see Ehlers-Danlos syndrome, vascular type
- SADDAN
- Sarcoma, breast, leukemia, and adrenal gland (SBLA) syndrome see Li-Fraumeni syndrome
- Sarcoma family syndrome of Li and Fraumeni see Li-Fraumeni syndrome
- SBLA syndrome see Li-Fraumeni syndrome
- SBMA see spinal and bulbar muscular atrophy
- SCD see sickle cell anemia
- Schwannoma, Acoustic, Bilateral see neurofibromatosis 2
- SCIDX1 see X-linked severe combined immunodeficiency
- sclerosis tuberosa see tuberous sclerosis
- SDAT see Alzheimer disease
- SED congenita see spondyloepiphyseal dysplasia congenita
- SED Strudwick see spondyloepimetaphyseal dysplasia, Strudwick type
- SEDc see spondyloepiphyseal dysplasia congenita
- Sedlackova syndrome see 22q11.2 deletion syndrome
- SEMD, Strudwick type see spondyloepimetaphyseal dysplasia, Strudwick type
- Senile Dementia see Alzheimer disease, type 2
- Severe achondroplasia with developmental delay and acanthosis nigricans see SADDAN
- Shprintzen syndrome see 22q11.2 deletion syndrome
- sickle cell anemia
- Skeleton-skin-brain syndrome see SADDAN
- Skin Diseases see Birt-Hogg-Dubé syndrome
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Skin Pigmentation Disorders
- SMA see spinal muscular atrophy
- SMED, Strudwick type see spondyloepimetaphyseal dysplasia, Strudwick type
- SMED, type I see spondyloepimetaphyseal dysplasia, Strudwick type
- South African genetic porphyria see variegate porphyria
- spastic paralysis, infantile onset ascending see infantile-onset ascending hereditary spastic paralysis
- SPD see spondyloperipheral dysplasia
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Speech and Communication Disorders
- Sphingolipidosis, Tay-Sachs see Tay-Sachs disease
- Sphingomyelin/cholesterol lipidosis see Niemann-Pick disease
- Sphingomyelin lipidosis see Niemann-Pick disease
- Sphingomyelinase deficiency see Niemann-Pick disease
- spinal and bulbar muscular atrophy
- spinal muscular atrophy
- spinal muscular atrophy, distal type V see distal spinal muscular atrophy, type V
- spinal muscular atrophy, distal, with upper limb predominance see distal spinal muscular atrophy, type V
- Spinocerebellar Ataxia, Friedreich see Friedreich ataxia
- spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloepiphyseal dysplasia see collagenopathy, types II and XI
- spondyloepiphyseal dysplasia congenita
- Spondylometaepiphyseal dysplasia congenita, Strudwick type see spondyloepimetaphyseal dysplasia, Strudwick type
- Spondylometaphyseal dysplasia (SMD) see spondyloepimetaphyseal dysplasia, Strudwick type
- Spondylometaphyseal Dysplasia, Strudwick Type see spondyloepimetaphyseal dysplasia, Strudwick type
- spondyloperipheral dysplasia
- Spongy degeneration of central nervous system see Canavan disease
- Spongy degeneration of the brain see Canavan disease
- Spongy degeneration of white matter in infancy see Canavan disease
- sporadic primary pulmonary hypertension see primary pulmonary hypertension
- SSB syndrome see SADDAN
- Stale fish syndrome see trimethylaminuria
- Steely Hair Syndrome see Menkes syndrome
- Steinert disease see myotonic dystrophy
- Steinert myotonic dystrophy syndrome see myotonic dystrophy
- Stickler syndrome
- Stroke see CADASIL
- Strudwick syndrome see spondyloepimetaphyseal dysplasia, Strudwick type
- Subacute Neuronopathic Gaucher Disease see Gaucher disease, type 3
- Surdo-cardiac syndrome see Jervell and Lange-Nielsen syndrome
- Swedish genetic porphyria see acute intermittent porphyria
- Swedish porphyria see acute intermittent porphyria
- Swiss cheese cartilage dysplasia see Kniest dysplasia
- 5p- Syndrome see cri-du-chat syndrome
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