MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

21q22.11q22.12 microdeletion syndrome

ORPHA:261323Malf.
Not applicable

22q11.2 deletion syndrome

ORPHA:567Malf.
Autosomal dominant

22q11.2 duplication syndrome

ORPHA:1727Malf.
Autosomal dominant

2p13.2 microdeletion syndrome

ORPHA:363680Malf.
Autosomal dominant

2p15p16.1 microdeletion syndrome

ORPHA:261349Malf.
Not applicable

2p21 microdeletion syndrome without cystinuria

ORPHA:369881Malf.
Autosomal recessive

2p25.3 microduplication syndrome

ORPHA:699850Malf.
Autosomal dominant

2q13 microdeletion syndrome

ORPHA:684742Malf.
Autosomal dominant

2q23.1 microdeletion syndrome

ORPHA:228402Malf.
Not applicable, Unknown

2q23.1 microduplication syndrome

ORPHA:313947Malf.
Not applicable, Unknown

2q31.1 microdeletion syndrome

ORPHA:251014Malf.
Not applicable, Unknown

2q32q33 deletion syndrome

ORPHA:251019Malf.
Not applicable, Unknown

2q37 microdeletion syndrome

ORPHA:1001Malf.
Autosomal dominant, Not applicable

3C syndrome

ORPHA:7Malf.
Autosomal recessive, X-linked recessive

3M syndrome

ORPHA:2616Malf.
Autosomal recessive

3MC syndrome

ORPHA:293843Malf.
Autosomal recessive

3p25.3 microdeletion syndrome

ORPHA:435638Malf.
Not applicable

3q13 microdeletion syndrome

ORPHA:1621Malf.
Not applicable

3q26 microduplication syndrome

ORPHA:96095Malf.

3q26q28 deletion syndrome

ORPHA:695611Malf.
Autosomal dominant

3q29 microdeletion syndrome

ORPHA:65286Malf.
Autosomal dominant

3q29 microduplication syndrome

ORPHA:251038Malf.
Autosomal dominant, Not applicable

45,X/46,XY mixed gonadal dysgenesis

ORPHA:1772Malf.
Not applicable, Unknown

46,XX difference of sex development-anorectal anomalies syndrome

ORPHA:2973Malf.