Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Bullous impetigo
Not applicable
All ages
Bullous lichen planus
Autosomal dominant, Not applicable
Childhood
Bullous pemphigoid
Not applicable
All ages
Burkitt lymphoma
Not applicable
All ages
Burning mouth syndrome
Adult
Butterfly-shaped pigment dystrophy
Autosomal dominant
Adult
C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
Autosomal recessive
Infancy
CACH syndrome
Autosomal recessive
Childhood
CAD-CDG
Autosomal recessive
Infancy
CADDS
X-linked recessive
Infancy, Neonatal
CADINS disease
Autosomal dominant
CANOMAD syndrome
Adult, Elderly
CARD8-related inflammatory bowel disease
Autosomal dominant
CCDC115-CDG
Autosomal recessive
Infancy, Neonatal
CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome
Autosomal dominant
Neonatal
CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome
Autosomal dominant
Childhood, Infancy
CDKL5-deficiency disorder
X-linked dominant
Infancy, Neonatal
CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome
Autosomal recessive
Adolescent, Neonatal
CEDNIK syndrome
Autosomal recessive
Infancy, Neonatal
CELSR1-related late-onset primary lymphedema
Autosomal dominant
Adolescent, Childhood, Infancy, Neonatal
CHD4-related neurodevelopmental disorder
Autosomal dominant
Childhood, Infancy
CHD8 overgrowth syndrome
Autosomal dominant
No data available
CHILD syndrome
X-linked dominant
Antenatal, Infancy, Neonatal
CHST3-related skeletal dysplasia
Autosomal recessive
Antenatal, Neonatal