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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 (Malform.) Сброс

46,XX difference of sex development-skeletal anomalies syndrome

ORPHA:2975Malform.
Unknown

46,XX gonadal dysgenesis

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

46,XX ovotesticular difference of sex development

ORPHA:2138Malform.
Autosomal dominant, Autosomal recessive

46,XX testicular difference of sex development

ORPHA:393Malform.
Autosomal dominant

46,XY complete gonadal dysgenesis

ORPHA:242Malform.
Autosomal dominant, Autosomal recessive, X-linked recessive, Y-linked

46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome

ORPHA:168563Malform.
Autosomal recessive

46,XY partial gonadal dysgenesis

ORPHA:251510Malform.
Autosomal dominant, Autosomal recessive, X-linked recessive, Y-linked

47,XYY syndrome

ORPHA:8Malform.
Not applicable

48,XXXY syndrome

ORPHA:96263Malform.
Not applicable, Unknown

48,XXYY syndrome

ORPHA:10Malform.
Not applicable, Unknown

48,XYYY syndrome

ORPHA:99329Malform.

49,XXXXY syndrome

ORPHA:96264Malform.
Not applicable, Unknown

49,XXXYY syndrome

ORPHA:261534Malform.

49,XYYYY syndrome

ORPHA:99330Malform.

4p16.3 microduplication syndrome

ORPHA:96072Malform.

4q21 microdeletion syndrome

ORPHA:238750Malform.
Not applicable, Unknown

4q25 proximal deletion syndrome

ORPHA:502437Malform.

5p13 microduplication syndrome

ORPHA:329802Malform.
Not applicable, Unknown

5q35 microduplication syndrome

ORPHA:228415Malform.
Not applicable, Unknown

6p22 microdeletion syndrome

ORPHA:251046Malform.
Not applicable, Unknown

6q terminal deletion syndrome

ORPHA:75857Malform.
Not applicable, Unknown

6q25.2q25.3 microdeletion syndrome

ORPHA:251056Malform.
Not applicable

7p22.1 microduplication syndrome

ORPHA:314034Malform.
Autosomal recessive

7q11.23 microduplication syndrome

ORPHA:96121Malform.