Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Terminal osseous dysplasia-pigmentary defects syndrome
X-linked dominant
Infancy, Neonatal
Tetraamelia-multiple malformations syndrome
Autosomal recessive, X-linked recessive
Antenatal, Infancy, Neonatal
Tetragametic chimerism syndrome
Not applicable, Unknown
Infancy, Neonatal
Tetralogy of Fallot
Autosomal dominant, Multigenic/multifactorial
Antenatal, Neonatal
Tetramelic monodactyly
Autosomal dominant
Antenatal
Tetraploidy syndrome
Antenatal, Neonatal
Tetrasomy 18p syndrome
Not applicable
Antenatal, Neonatal
Tetrasomy 21 syndrome
Antenatal, Infancy, Neonatal
Tetrasomy 5p syndrome
Antenatal, Neonatal
Tetrasomy 9p syndrome
Antenatal, Neonatal
Tetrasomy X syndrome
Infancy, Neonatal
Thakker-Donnai syndrome
Autosomal recessive
Antenatal, Neonatal
Thalidomide embryopathy
Not applicable
Antenatal, Neonatal
Thickened earlobes-conductive deafness syndrome
Autosomal dominant
All ages
Thin ribs-tubular bones-dysmorphism syndrome
Neonatal
Thomas syndrome
Autosomal recessive
Antenatal, Neonatal
Thoracic dysplasia-hydrocephalus syndrome
Antenatal
Thoraco-abdominal enteric duplication
Infancy
Thoracolaryngopelvic dysplasia
Autosomal dominant
Infancy, Neonatal
Thrombocytopenia-absent radius syndrome
Autosomal recessive
Antenatal, Neonatal
Thumb deformity-alopecia-pigmentation anomaly syndrome
Infancy, Neonatal
Thumb stiffness-brachydactyly-intellectual disability syndrome
Autosomal dominant
Infancy, Neonatal
Thymic-renal-anal-lung dysplasia
Autosomal recessive
Antenatal, Neonatal
Thyrocerebrorenal syndrome
Autosomal recessive
Childhood