Shiga toxin-associated hemolytic uremic syndrome

Not applicable

All ages

Short stature due to growth hormone qualitative anomaly

Autosomal recessive

Infancy, Neonatal

Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia

X-linked recessive

Infancy, Neonatal

Sickle cell S-D Punjab disease

Autosomal recessive

All ages

Sickle cell S-E disease

Autosomal recessive

All ages

Sickle cell S-Lepore disease

Sickle cell S-O Arab disease

Sickle cell S-other specified hemoglobin variant

Single-organ polyarteritis nodosa

Not applicable

Single-system multifocal Langerhans cell histiocytosis

Not applicable

Sporadic porphyria cutanea tarda

Multigenic/multifactorial

Stevens-Johnson syndrome

Not applicable

All ages

Stickler syndrome type 1

Autosomal dominant

Childhood, Infancy, Neonatal

Stickler syndrome type 2

Autosomal dominant

Childhood, Infancy, Neonatal

Streptococcus pneumoniae-associated hemolytic uremic syndrome

All ages

Sub-cortical nodular heterotopia

Antenatal, Infancy, Neonatal

Subependymal nodular heterotopia

Antenatal, Infancy, Neonatal

Synpolydactyly type 1

Autosomal dominant

Synpolydactyly type 2

Autosomal dominant

Systemic polyarteritis nodosa

Not applicable

Tay-Sachs disease, adult form

Autosomal recessive

Tay-Sachs disease, infantile form

Autosomal recessive

Tay-Sachs disease, juvenile form

Autosomal recessive

Telangiectasia macularis eruptiva perstans

Unknown