Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Didymosis aplasticosebacea
Not applicable
Infancy, Neonatal
Diencephalic syndrome
Not applicable
Adolescent, Adult, Childhood, Infancy
Diencephalic-mesencephalic junction dysplasia
Autosomal recessive
Antenatal, Neonatal
Dietary iron overload disease
Not applicable
Adult, Elderly
Diethylstilbestrol syndrome
Not applicable
All ages
Difference of sex development-intellectual disability syndrome
Unknown
Neonatal
Differentiated thyroid carcinoma
Not applicable
Adolescent, Adult, Childhood
Diffuse alveolar hemorrhage
Not applicable
Adolescent, Adult, Childhood, Elderly, Infancy
Diffuse astrocytoma
Adolescent, Adult, Childhood
Diffuse capillary malformation with overgrowth
Not applicable
Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome
Autosomal recessive
Infancy, Neonatal
Diffuse cutaneous mastocytosis
Not applicable
Infancy, Neonatal
Diffuse cutaneous systemic sclerosis
Multigenic/multifactorial, Not applicable
Adult
Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
Adult, Elderly
Diffuse intrinsic pontine glioma
All ages
Diffuse large B-cell lymphoma
Multigenic/multifactorial, Not applicable
Adult
Diffuse large B-cell lymphoma of the central nervous system
Multigenic/multifactorial, Not applicable
Diffuse lymphatic malformation
Not applicable
Infancy, Neonatal
Diffuse palmoplantar keratoderma with painful fissures
Autosomal dominant
Infancy, Neonatal
Diffuse palmoplantar keratoderma, Bothnian type
Autosomal dominant
Childhood, Infancy
Diffuse palmoplantar keratoderma-acrocyanosis syndrome
Autosomal dominant
Infancy, Neonatal
Diffuse panbronchiolitis
Multigenic/multifactorial
Adult
Digenic Alport syndrome
Autosomal dominant, Autosomal recessive