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"

29 matching diseasesClear search ×

Kagami-Ogata syndrome due to maternal 14q32.2 microdeletion

Maternal del(14)(q32.2) · Maternal monosomy 14q32.2

ORPHA:254528

14q11.2 microdeletion syndrome

Del(14)(q11.2) · Monosomy 14q11.2

ORPHA:261120

14q22q23 microdeletion syndrome

14q22-q23 microdeletion syndrome · Del(14)(q22q23)

ORPHA:264200

14q24.1q24.3 microdeletion syndrome

Del(14)(q24.1q24.3) · Monosomy 14q24.1q24.3

ORPHA:401935

15q11.2 microdeletion syndrome

15q11.2 BP1-BP2 microdeletion syndrome · Del(15)(q11.2)

ORPHA:261183

16p11.2p12.2 microdeletion syndrome

Del(16)(p11.2p12.2) · Monosomy 16p11.2p12.2

ORPHA:261211

17q23.1q23.2 microdeletion syndrome

Del(17)(q23.1q23.2) · Monosomy 17q23.1q23.2

ORPHA:261279

1p31p32 microdeletion syndrome

Del(1)(p31p32) · Monosomy 1p31p32

ORPHA:401986

1p35.2 microdeletion syndrome

Deletion 1p35.2 · Del(1)(p35.2)

ORPHA:456298

1p36 deletion syndrome

Del(1)(p36) · Deletion 1p36

ORPHA:1606

2q23.1 microdeletion syndrome

Del(2)(q23.1) · Monosomy 2q23.1

ORPHA:228402

2q31.1 microdeletion syndrome

Del(2)(q31.1) · Monosomy 2q31.1

ORPHA:251014

2q32q33 deletion syndrome

Monosomy 2q32q33 · Del(2)(q32q33)

ORPHA:251019

8p11.2 deletion syndrome

Del(8)(p11.2) · Monosomy 8p11.2

ORPHA:251066

Anophthalmia-hypothalamo-pituitary insufficiency syndrome

14q22 microdeletion syndrome · Al Frayh-Facharzt-Haque syndrome

ORPHA:1102

Distal 16p11.2 microdeletion syndrome

Distal del(16)(p11.2) · Distal monosomy 16p11.2

ORPHA:261222

Distal deletion 10p syndrome

Distal monosomy 10p · Monosomy 10pter

ORPHA:1580

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 14q syndrome

Distal monosomy 14q · Telomeric deletion 14q

ORPHA:96150

Distal deletion 17q syndrome

Distal monosomy 17q · Monosomy 17qter

ORPHA:1597

Distal deletion 1q syndrome

Distal monosomy 1q · Monosomy 1qter

ORPHA:36367

DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion

21q22.13q22.2 microdeletion syndrome · Del(21)(q22.13q22.2)

ORPHA:268261

FOXG1 syndrome due to 14q12 microdeletion

Del(14)(q12) · Monosomy 14q12

ORPHA:261144

Hao-Fountain syndrome due to 16p13.2 microdeletion

Del(16)(p13.2) · Monosomy 16p13.2

ORPHA:500055

Jacobsen syndrome

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

ORPHA:2308

Paternal 20q13.2q13.3 microdeletion syndrome

Paternal del(20)(q13.2q13.3) · Paternal monosomy 20q13.2q13.3

ORPHA:261304

SATB2-associated syndrome due to a chromosomal rearrangement

Del(2)(q33.1) · Monosomy 2q33.1

ORPHA:251028