Synpolydactyly type 2

Autosomal dominant

Syringocystadenoma papilliferum

Unknown

Adolescent, Childhood, Infancy, Neonatal

Syringomyelia

Not applicable

All ages

Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood

Not applicable

Childhood

Systemic capillary leak syndrome

Not applicable

Adult

Systemic diseases with anterior uveitis

Adolescent, Adult, Childhood, Elderly

Systemic lupus erythematosus

Not applicable

Adolescent, Adult, Childhood, Infancy

Systemic mastocytosis

Not applicable

All ages

Systemic mastocytosis with associated hematologic neoplasm

Not applicable

Adult, Elderly

Systemic monochloroacetate poisoning

All ages

Systemic polyarteritis nodosa

Not applicable

Systemic primary carnitine deficiency

Autosomal recessive

Infancy, Neonatal

Systemic sclerosis

Multigenic/multifactorial, Not applicable

Adult

Systemic-onset juvenile idiopathic arthritis

Multigenic/multifactorial, Unknown

Childhood

Sézary syndrome

Multigenic/multifactorial, Not applicable

Adult

T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta

Autosomal recessive

Infancy

T-B+ severe combined immunodeficiency due to CD45 deficiency

Autosomal recessive

Infancy

T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency

Autosomal recessive

Infancy

T-B+ severe combined immunodeficiency due to JAK3 deficiency

Autosomal recessive

Infancy, Neonatal

T-B+ severe combined immunodeficiency due to gamma chain deficiency

X-linked recessive

Neonatal

T-cell immunodeficiency with epidermodysplasia verruciformis

Autosomal recessive

Childhood

T-cell immunodeficiency with thymic aplasia

Autosomal recessive

Infancy, Neonatal

T-cell large granular lymphocyte leukemia

Not applicable

Adult

T-cell non-Hodgkin lymphoma