Rare (orphan) diseases
The full catalogue of 7,547 diseases with genetics, phenotypes, epidemiology, orphan drugs, and clinical trials.
Kindler epidermolysis bullosa
Autosomal recessive
Infancy, Neonatal
Kjellin syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Kleine-Levin syndrome
Adolescent, Adult, Childhood
Kniest dysplasia
Autosomal dominant
Antenatal, Infancy, Neonatal
Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
Autosomal dominant
Childhood
Kostmann syndrome
Autosomal recessive
Neonatal
Krabbe disease
Autosomal recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Kufor-Rakeb syndrome
Autosomal recessive
Adolescent, Childhood
Kuru
Multigenic/multifactorial, Not applicable
All ages
Kyasanur forest disease
All ages
Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome
Autosomal recessive
Infancy, Neonatal
Kyphoscoliotic Ehlers-Danlos syndrome
Antenatal, Neonatal
Kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome
Autosomal recessive
Childhood, Infancy, Neonatal
L-2-hydroxyglutaric aciduria
Autosomal recessive
Childhood
L-Arginine:glycine amidinotransferase deficiency
Autosomal recessive
Infancy
LAMA5-related multisystemic syndrome
Autosomal dominant
Infancy, Neonatal
LCAT deficiency
Autosomal recessive
All ages
LIG4 syndrome
Autosomal recessive
Infancy, Neonatal
LIPE-related familial partial lipodystrophy
Autosomal recessive
Adult
LMNA-related cardiocutaneous progeria syndrome
Autosomal dominant
Childhood
La Crosse encephalitis
Not applicable
All ages
Lafora disease
Autosomal recessive
Adolescent, Childhood
Laing distal myopathy
Autosomal dominant
Childhood
Lamb-Shaffer syndrome
Autosomal dominant
Infancy