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

21q22.11q22.12 microdeletion syndrome

ORPHA:261323Malform.
Not applicable

22q11.2 deletion syndrome

ORPHA:567Malform.
Autosomal dominant

22q11.2 duplication syndrome

ORPHA:1727Malform.
Autosomal dominant

2p13.2 microdeletion syndrome

ORPHA:363680Malform.
Autosomal dominant

2p15p16.1 microdeletion syndrome

ORPHA:261349Malform.
Not applicable

2p21 microdeletion syndrome without cystinuria

ORPHA:369881Malform.
Autosomal recessive

2p25.3 microduplication syndrome

ORPHA:699850Malform.
Autosomal dominant

2q13 microdeletion syndrome

ORPHA:684742Malform.
Autosomal dominant

2q23.1 microdeletion syndrome

ORPHA:228402Malform.
Not applicable, Unknown

2q23.1 microduplication syndrome

ORPHA:313947Malform.
Not applicable, Unknown

2q31.1 microdeletion syndrome

ORPHA:251014Malform.
Not applicable, Unknown

2q32q33 deletion syndrome

ORPHA:251019Malform.
Not applicable, Unknown

2q37 microdeletion syndrome

ORPHA:1001Malform.
Autosomal dominant, Not applicable

3C syndrome

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

3M syndrome

ORPHA:2616Malform.
Autosomal recessive

3MC syndrome

ORPHA:293843Malform.
Autosomal recessive

3p25.3 microdeletion syndrome

ORPHA:435638Malform.
Not applicable

3q13 microdeletion syndrome

ORPHA:1621Malform.
Not applicable

3q26 microduplication syndrome

ORPHA:96095Malform.

3q26q28 deletion syndrome

ORPHA:695611Malform.
Autosomal dominant

3q29 microdeletion syndrome

ORPHA:65286Malform.
Autosomal dominant

3q29 microduplication syndrome

ORPHA:251038Malform.
Autosomal dominant, Not applicable

45,X/46,XY mixed gonadal dysgenesis

ORPHA:1772Malform.
Not applicable, Unknown

46,XX difference of sex development-anorectal anomalies syndrome

ORPHA:2973Malform.