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

Diaphragmatic hernia-short bowel-asplenia syndrome

ORPHA:527468Malf.
Autosomal recessive

Diethylstilbestrol syndrome

ORPHA:1916Malf.
Not applicable

Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome

ORPHA:404437Malf.
Autosomal recessive

Diffuse lymphatic malformation

ORPHA:141209Malf.
Not applicable

Digital extensor muscle aplasia-polyneuropathy

ORPHA:2926Malf.

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

ORPHA:2229Malf.
Autosomal recessive

Dislocation of the hip-dysmorphism syndrome

ORPHA:2412Malf.
Autosomal recessive

Distal 16p11.2 microdeletion syndrome

ORPHA:261222Malf.
Not applicable

Distal 17p13.1 microdeletion syndrome

ORPHA:319171Malf.
Not applicable

Distal 17p13.3 microdeletion syndrome

ORPHA:261257Malf.
Not applicable

Distal 22q11.2 microdeletion syndrome

ORPHA:261330Malf.
Autosomal dominant

Distal 22q11.2 microduplication syndrome

ORPHA:261337Malf.
Autosomal dominant

Distal 7q11.23 microdeletion syndrome

ORPHA:254351Malf.
Autosomal dominant, Not applicable

Distal 7q11.23 microduplication syndrome

ORPHA:261102Malf.

Distal Xq28 microduplication syndrome

ORPHA:293939Malf.
X-linked recessive

Distal arthrogryposis type 1

ORPHA:1146Malf.
Autosomal dominant

Distal arthrogryposis type 10

ORPHA:251515Malf.
Autosomal dominant

Distal arthrogryposis-progressive scoliosis-thumb deformity-impaired proprioception syndrome

ORPHA:707937Malf.
Autosomal recessive

Distal deletion 10q syndrome

ORPHA:96148Malf.
Not applicable, Unknown

Distal deletion 12p syndrome

ORPHA:280325Malf.

Distal deletion 12q syndrome

ORPHA:96149Malf.

Distal deletion 13q syndrome

ORPHA:1590Malf.

Distal deletion 14q syndrome

ORPHA:96150Malf.

Distal deletion 15q syndrome

ORPHA:1596Malf.