Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

22 matching diseasesClear search ×

12q15q21 microdeletion syndrome

Del(12)(q15)(q21) · Deletion 12q15q21

ORPHA:289513

10p13-p14 deletion syndrome

Del(10)(p13p14) · Deletion 10p13-p14

ORPHA:687695

12q14 microdeletion syndrome

Del(12)(q14) · Deletion 12q14

ORPHA:94063

1p35.2 microdeletion syndrome

Deletion 1p35.2 · Del(1)(p35.2)

ORPHA:456298

1p36 deletion syndrome

Del(1)(p36) · Deletion 1p36

ORPHA:1606

2q37 microdeletion syndrome

Albright hereditary osteodystrophy type 3 · Albright hereditary osteodystrophy-like syndrome

ORPHA:1001

3q29 microdeletion syndrome

3q subtelomere deletion syndrome · 3qter deletion

ORPHA:65286

8q21.11 microdeletion syndrome

Del(8)(q21.11) · Deletion 8q21.11

ORPHA:284160

8q24.3 microdeletion syndrome

Del(8)(q24.3) · Deletion 8q24.3

ORPHA:508488

Distal deletion 10q syndrome

Distal monosomy 10q · Monosomy 10qter

ORPHA:96148

Distal deletion 12q syndrome

Distal monosomy 12q · Monosomy 12qter

ORPHA:96149

Distal deletion 13q syndrome

Distal monosomy 13q · 13q32 deletion

ORPHA:1590

Distal deletion 15q syndrome

Distal monosomy 15q · 15q26 deletion syndrome

ORPHA:1596

Jacobsen syndrome

Chromosome 11q deletion syndrome · Del(11)(q23.3)

ORPHA:2308

Monosomy 13q14 syndrome

Del(13)(q14) · Deletion 13q14

ORPHA:1587

Monosomy 18q syndrome

18q- syndrome · Deletion 18q

ORPHA:1600

Monosomy 22 syndrome

Del(22) · Deletion 22

ORPHA:96123

Monosomy 5p syndrome

Cri du chat syndrome · Deletion 5p

ORPHA:281

Phelan-McDermid syndrome due to 22q13.3 deletion

22q13.3 deletion · Chromosome 22q13.3 deletion syndrome

ORPHA:662169

Potocki-Shaffer syndrome

11p11.2 deletion · Proximal 11p deletion syndrome

ORPHA:52022

WAGR syndrome

Del(11)(p13) · Deletion 11p13

ORPHA:893

ZMYND11-related developmental delay-speech delay-seizures-behavioral abnormalities-craniofacial dysmorphism syndrome due to 10p15.3 microdeletion

10p15.3 microdeletion syndrome · Del(10)(p15.3)

ORPHA:687424