Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Kindler epidermolysis bullosa
Autosomal recessive
Infancy, Neonatal
King-Denborough syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Kjellin syndrome
Autosomal recessive
Adolescent, Adult, Childhood
Kleefstra syndrome
Autosomal dominant
Neonatal
Kleefstra syndrome due to 9q34 microdeletion
Not applicable
Infancy, Neonatal
Kleefstra syndrome due to a point mutation
Autosomal dominant
Neonatal
Kleine-Levin syndrome
Adolescent, Adult, Childhood
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
Autosomal recessive
Infancy
Kniest dysplasia
Autosomal dominant
Antenatal, Infancy, Neonatal
Knobloch syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
Autosomal dominant
Childhood
Kommerell diverticulum
Not applicable
Koolen-De Vries syndrome
Autosomal dominant
Antenatal, Infancy, Neonatal
Koolen-De Vries syndrome due to a point mutation
Autosomal dominant
Infancy, Neonatal
Kosaki overgrowth syndrome
No data available
Infancy
Kostmann syndrome
Autosomal recessive
Neonatal
Kousseff syndrome
Antenatal, Infancy, Neonatal
Krabbe disease
Autosomal recessive
Adolescent, Adult, Childhood, Infancy, Neonatal
Kufor-Rakeb syndrome
Autosomal recessive
Adolescent, Childhood
Kuru
Multigenic/multifactorial, Not applicable
All ages
Kuskokwim syndrome
Autosomal recessive
Childhood, Neonatal
Kyasanur forest disease
All ages
Kyphomelic dysplasia
Antenatal, Neonatal
Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome
Autosomal recessive
Infancy, Neonatal