MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Diaphragmatic hernia-short bowel-asplenia syndrome

ORPHA:527468Malform.
Autosomal recessive

Diethylstilbestrol syndrome

ORPHA:1916Malform.
Not applicable

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

ORPHA:404437Malform.
Autosomal recessive

Diffuse lymphatic malformation

ORPHA:141209Malform.
Not applicable

Digital extensor muscle aplasia-polyneuropathy

ORPHA:2926Malform.

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

ORPHA:2229Malform.
Autosomal recessive

Dislocation of the hip-dysmorphism syndrome

ORPHA:2412Malform.
Autosomal recessive

Distal 16p11.2 microdeletion syndrome

ORPHA:261222Malform.
Not applicable

Distal 17p13.1 microdeletion syndrome

ORPHA:319171Malform.
Not applicable

Distal 17p13.3 microdeletion syndrome

ORPHA:261257Malform.
Not applicable

Distal 22q11.2 microdeletion syndrome

ORPHA:261330Malform.
Autosomal dominant

Distal 22q11.2 microduplication syndrome

ORPHA:261337Malform.
Autosomal dominant

Distal 7q11.23 microdeletion syndrome

ORPHA:254351Malform.
Autosomal dominant, Not applicable

Distal 7q11.23 microduplication syndrome

ORPHA:261102Malform.

Distal Xq28 microduplication syndrome

ORPHA:293939Malform.
X-linked recessive

Distal arthrogryposis type 1

ORPHA:1146Malform.
Autosomal dominant

Distal arthrogryposis type 10

ORPHA:251515Malform.
Autosomal dominant

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

ORPHA:707937Malform.
Autosomal recessive

Distal deletion 10q syndrome

ORPHA:96148Malform.
Not applicable, Unknown

Distal deletion 12p syndrome

ORPHA:280325Malform.

Distal deletion 12q syndrome

ORPHA:96149Malform.

Distal deletion 13q syndrome

ORPHA:1590Malform.

Distal deletion 14q syndrome

ORPHA:96150Malform.

Distal deletion 15q syndrome

ORPHA:1596Malform.