Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Autosomal dominant, Autosomal recessive
Infancy
Hypotonia with lactic acidemia and hyperammonemia
Autosomal recessive
Antenatal, Neonatal
Hypotonia-cystinuria syndrome
Autosomal recessive
Infancy, Neonatal
Hypotonia-failure to thrive-microcephaly syndrome
Autosomal recessive
Infancy, Neonatal
Hypotonia-speech impairment-severe cognitive delay syndrome
Autosomal recessive
Infancy, Neonatal
Hypotrichosis simplex
Autosomal dominant, Autosomal recessive
Childhood
Hypotrichosis simplex of the scalp
Autosomal dominant
Childhood
Hypotrichosis-deafness syndrome
Autosomal dominant
Infancy, Neonatal
Hypotrichosis-intellectual disability, Lopes type
Autosomal recessive
Childhood, Infancy
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
Infancy, Neonatal
Hypoxanthine guanine phosphoribosyltransferase partial deficiency
X-linked recessive
All ages
ICHAD syndrome
Autosomal dominant
IFIH1-related hereditary spastic paraplegia
Autosomal dominant
IL21-related infantile inflammatory bowel disease
Autosomal recessive
Infancy
IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome
Autosomal dominant
Childhood, Infancy, Neonatal
IRIDA syndrome
Autosomal recessive
Infancy, Neonatal
IRVAN syndrome
Not applicable
Adolescent, Adult, Childhood
ISPD-related limb-girdle muscular dystrophy R20
Autosomal recessive
Childhood, Infancy
ITM2B amyloidosis
Autosomal dominant
Adult
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
Autosomal recessive
Infancy, Neonatal
Iatrogenic Creutzfeldt-Jakob disease
Adult
Ichthyosis follicularis-alopecia-photophobia syndrome
Autosomal dominant, Not applicable, X-linked recessive
Infancy, Neonatal
Ichthyosis hystrix of Curth-Macklin
Autosomal dominant, Not applicable
Childhood