Laminin subunit alpha 2-related limb-girdle muscular dystrophy R23

Autosomal recessive

Laminopathy with lipodystrophy

Laminopathy with peripheral neuropathy

Laminopathy with premature aging

Laminopathy with striated muscle involvement

Landau-Kleffner syndrome

Autosomal dominant, Unknown

Childhood

Langer mesomelic dysplasia

Autosomal recessive

Antenatal

Langerhans cell histiocytosis

Unknown

All ages

Langerhans cell sarcoma

All ages

Large granular lymphocyte leukemia

Large/giant congenital melanocytic nevus

Multigenic/multifactorial

Infancy, Neonatal

Laron syndrome

Autosomal recessive

Infancy, Neonatal

Laron syndrome with immunodeficiency

Autosomal dominant, Autosomal recessive

Childhood, Infancy, Neonatal

Larsen syndrome

Autosomal dominant

Antenatal, Infancy, Neonatal

Larsen-like osseous dysplasia-short stature syndrome

Neonatal

Larsen-like syndrome, B3GAT3 type

Autosomal recessive

Infancy, Neonatal

Laryngeal abductor paralysis

Neonatal

Laryngeal abductor paralysis-intellectual disability syndrome

X-linked recessive

Childhood

Laryngeal neuroendocrine tumor

Adult

Laryngo-onycho-cutaneous syndrome

Autosomal recessive

Infancy, Neonatal

Laryngocele

All ages

Laryngotracheoesophageal cleft

Autosomal dominant, Not applicable

Antenatal, Neonatal

Laryngotracheoesophageal cleft type 0

Laryngotracheoesophageal cleft type 1

Infancy, Neonatal