Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Trichodental syndrome
Autosomal dominant
Childhood
Trichodermodysplasia-dental alterations syndrome
Neonatal
Trichodysplasia-amelogenesis imperfecta syndrome
X-linked recessive
Infancy, Neonatal
Trichodysplasia-xeroderma syndrome
Neonatal
Trichofolliculoma
Not applicable
Adult
Trichohepatoenteric syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
Autosomal recessive
Infancy, Neonatal
Trichoodontoonychial dysplasia
Autosomal recessive
Infancy, Neonatal
Trichorhinophalangeal syndrome type 1
Autosomal dominant
Infancy, Neonatal
Trichorhinophalangeal syndrome type 2
Autosomal dominant
Childhood, Infancy, Neonatal
Trichothiodystrophy
Autosomal recessive, X-linked recessive
Infancy, Neonatal
Tricuspid atresia
Not applicable
Antenatal, Neonatal
Trigeminal neuralgia
Not applicable
Adolescent, Adult, Elderly
Trigeminal trophic syndrome
Adult, Elderly
Triglyceride deposit cardiomyovasculopathy
Autosomal recessive, Unknown
Trigonocephaly-bifid nose-acral anomalies syndrome
Unknown
Infancy, Neonatal
Trigonocephaly-broad thumbs syndrome
Autosomal dominant
Infancy, Neonatal
Trigonocephaly-short stature-developmental delay syndrome
Unknown
No data available
Triose phosphate-isomerase deficiency
Autosomal recessive
Neonatal
Triphalangeal thumbs-brachyectrodactyly syndrome
Autosomal dominant
Neonatal
Triple A syndrome
Autosomal recessive
All ages
Triploidy syndrome
Not applicable, Unknown
Antenatal, Neonatal
Trismus-pseudocamptodactyly syndrome
Autosomal dominant
Infancy, Neonatal
Trisomy 10p syndrome
Infancy, Neonatal