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"

200 matching diseasesClear search ×

1q21.1 microduplication syndrome

Dup(1)(q21.1) · Trisomy 1q21.1

ORPHA:250994

1q41q42 microdeletion syndrome

Del(1)(q41q42) · Monosomy 1q41q42

ORPHA:250999

1q44 microdeletion syndrome

Del(1)(q44) · Monosomy 1q44

ORPHA:238769

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

20q11.2 microdeletion syndrome

Del(20)(q11.2) · Monosomy 20q11

ORPHA:444051

20q11.2 microduplication syndrome

Dup(20)(q11.2)

ORPHA:363659

20q13.33 microdeletion syndrome

Del(20)(q13.33) · Monosomy 20q13.33

ORPHA:261311

21q deletion syndrome

21q- syndrome · Partial 21q monosomy

ORPHA:574

21q22.11q22.12 microdeletion syndrome

Del(21)(q22.11q22.12) · Monosomy 21q22.11q22.12

ORPHA:261323

22q11.2 deletion syndrome

22q11DS · CATCH 22

ORPHA:567

22q11.2 duplication syndrome

Dup(22)(q11) · Duplication 22q11.2

ORPHA:1727

2p13.2 microdeletion syndrome

Del(2)(p13.2)

ORPHA:363680

2p15p16.1 microdeletion syndrome

Del(2)(p15p16.1) · Monosomy 2p15p16.1

ORPHA:261349

2p21 microdeletion syndrome

2p21 deletion syndrome · Del(2)(p21)

ORPHA:163693

2p21 microdeletion syndrome without cystinuria

Del(2)(p21) without cystinuria

ORPHA:369881

2p25.3 microduplication syndrome

Trisomy 2p25.3 syndrome · Dup(2)(p25.3)

ORPHA:699850

2q13 microdeletion syndrome

del2q13 syndrome

ORPHA:684742

2q23.1 microdeletion syndrome

Del(2)(q23.1) · Monosomy 2q23.1

ORPHA:228402

2q23.1 microduplication syndrome

Dup(2)(q23.1) · Trisomy 2q23.1

ORPHA:313947

2q31.1 microdeletion syndrome

Del(2)(q31.1) · Monosomy 2q31.1

ORPHA:251014

2q32q33 deletion syndrome

Monosomy 2q32q33 · Del(2)(q32q33)

ORPHA:251019

2q37 microdeletion syndrome

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

ORPHA:1001

3p25.3 microdeletion syndrome

Del(3)p(25.3) · Intellectual disability-epilepsy-stereotypic hand movement syndrome

ORPHA:435638

3q13 microdeletion syndrome

Del(3)(q13) · Monosomy 3q13

ORPHA:1621

3q26 microduplication syndrome

Dup(3)(q26) · Trisomy 3q26

ORPHA:96095

3q26q27 microdeletion syndrome

Del(3)(q26q27) · Monosomy 3q26q27

ORPHA:356947

3q26q28 deletion syndrome

Del(3)(q26q28) · Monosomy 3q26q28 syndrome

ORPHA:695611

3q27.3 microdeletion syndrome

Del(3)(q27.3)

ORPHA:397695

3q29 microdeletion syndrome

3q subtelomere deletion syndrome · 3qter deletion

ORPHA:65286

3q29 microduplication syndrome

Trisomy 3q29

ORPHA:251038

46,XY difference of sex development due to impaired androgen production

46,XY DSD due to impaired androgen production · 46,XY disorder of sex development due to impaired androgen production

ORPHA:325357

4p16.3 microduplication syndrome

Distal duplication 4p · Distal trisomy 4p

ORPHA:96072

4q21 microdeletion syndrome

Del(4)(q21) · Monosomy 4q21

ORPHA:238750

4q25 proximal deletion syndrome

Proximal del(4)(q25) · Proximal monosomy 4q25

ORPHA:502437

5p13 microduplication syndrome

Dup(5)(p13) · Trisomy 5p13

ORPHA:329802

5q14.3 microdeletion syndrome

Del(5)(q14.3) · Monosomy 5q14.3

ORPHA:228384

5q22 microdeletion syndrome

Monosomy 5q22 syndrome · Del(5)(q22) syndrome

ORPHA:261584

5q35 microduplication syndrome

Dup(5)(q35) · Trisomy 5q35

ORPHA:228415

6p22 microdeletion syndrome

Del(6)(p22) · Monosomy 6p22

ORPHA:251046

6q terminal deletion syndrome

ORPHA:75857

6q16 microdeletion syndrome

Del(6)(q16) · Monosomy 6q16

ORPHA:171829

6q25.1 microdeletion syndrome

ORPHA:664404

6q25.2q25.3 microdeletion syndrome

Del(6)(q25.2q25.3) · Monosomy 6q25.2q25.3

ORPHA:251056

7p22.1 microduplication syndrome

Dup(7)(p22.1) · Trisomy 7p22.1

ORPHA:314034

7q11.23 microduplication syndrome

Dup(7)(q11.23) · Trisomy 7q11.23

ORPHA:96121

7q31 microdeletion syndrome

Del(7)(q31) · Monosomy 7q31

ORPHA:251061

8p inverted duplication/deletion syndrome

Invdupdel(8p) · Inverted 8p duplication/deletion syndrome

ORPHA:96092