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"

16 matching diseasesClear search ×

9p13 microdeletion syndrome

Del(9)(p13) · Monosomy 9p13

ORPHA:324313

10p13-p14 deletion syndrome

Del(10)(p13p14) · Deletion 10p13-p14

ORPHA:687695

12p12.1 microdeletion syndrome

Del(12)(p12.1) · Monosomy 12p12.1

ORPHA:313884

16p13.11 microdeletion syndrome

Del(16)(p13.11) · Monosomy 16p13.11

ORPHA:261236

19p13.12 microdeletion syndrome

Del(19)(p13.12) · Monosomy 19p13.12

ORPHA:254346

19p13.13 microdeletion syndrome

Del(19)(p13.13) · Monosomy 19p13.13

ORPHA:357001

20p12.3 microdeletion syndrome

Del(20)(p12.3) · Monosomy 20p12.3

ORPHA:261295

20p13 microdeletion syndrome

20p subtelomeric deletion syndrome · Del(20)(p13)

ORPHA:313781

2p13.2 microdeletion syndrome

Del(2)(p13.2)

ORPHA:363680

8p11.2 deletion syndrome

Del(8)(p11.2) · Monosomy 8p11.2

ORPHA:251066

Distal 17p13.1 microdeletion syndrome

Distal del(17)(p13.1)

ORPHA:319171

Distal 17p13.3 microdeletion syndrome

Distal del(17)(p13.3 ) · Distal monosomy 17p13.3

ORPHA:261257

Distal deletion 12p syndrome

12p13.33 microdeletion syndrome · Del(12)(p13.33)

ORPHA:280325

Hao-Fountain syndrome due to 16p13.2 microdeletion

Del(16)(p13.2) · Monosomy 16p13.2

ORPHA:500055

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