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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы
Найдено 1,772 заболеваний (Порок) Сброс

46,XX difference of sex development-skeletal anomalies syndrome

ORPHA:2975Порок
Unknown

46,XX gonadal dysgenesis

ORPHA:243Порок
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

46,XX ovotesticular difference of sex development

ORPHA:2138Порок
Autosomal dominant, Autosomal recessive

46,XX testicular difference of sex development

ORPHA:393Порок
Autosomal dominant

46,XY complete gonadal dysgenesis

ORPHA:242Порок
Autosomal dominant, Autosomal recessive, X-linked recessive, Y-linked

46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome

ORPHA:168563Порок
Autosomal recessive

46,XY partial gonadal dysgenesis

ORPHA:251510Порок
Autosomal dominant, Autosomal recessive, X-linked recessive, Y-linked

47,XYY syndrome

ORPHA:8Порок
Not applicable

48,XXXY syndrome

ORPHA:96263Порок
Not applicable, Unknown

48,XXYY syndrome

ORPHA:10Порок
Not applicable, Unknown

48,XYYY syndrome

ORPHA:99329Порок

49,XXXXY syndrome

ORPHA:96264Порок
Not applicable, Unknown

49,XXXYY syndrome

ORPHA:261534Порок

49,XYYYY syndrome

ORPHA:99330Порок

4p16.3 microduplication syndrome

ORPHA:96072Порок

4q21 microdeletion syndrome

ORPHA:238750Порок
Not applicable, Unknown

4q25 proximal deletion syndrome

ORPHA:502437Порок

5p13 microduplication syndrome

ORPHA:329802Порок
Not applicable, Unknown

5q35 microduplication syndrome

ORPHA:228415Порок
Not applicable, Unknown

6p22 microdeletion syndrome

ORPHA:251046Порок
Not applicable, Unknown

6q terminal deletion syndrome

ORPHA:75857Порок
Not applicable, Unknown

6q25.2q25.3 microdeletion syndrome

ORPHA:251056Порок
Not applicable

7p22.1 microduplication syndrome

ORPHA:314034Порок
Autosomal recessive

7q11.23 microduplication syndrome

ORPHA:96121Порок