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"

146 matching diseasesClear search ×

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

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

ORPHA:268261

Emanuel syndrome

Der(22)t(11;22) syndrome · Supernumerary der(22) syndrome

ORPHA:96170

Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion

Desanto-Shinawi syndrome due to 10p11.21p12.31 microdeletion · 10p12p11 microdeletion syndrome

ORPHA:284169

Facial dysmorphism-Intellectual disability-rhombencephalosynapsis syndrome

MN1 C-terminal truncation syndrome · MCTT

ORPHA:693549

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

Ichthyosis-short stature-brachydactyly-microspherophakia syndrome

15q26.3 microdeletion syndrome

ORPHA:363992

Kleefstra syndrome due to 9q34 microdeletion

9q subtelomeric deletion syndrome · 9qSTDS

ORPHA:96147

Lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster

Lethal 1p36.33 deletion syndrome

ORPHA:615986

Mesomelia-synostoses syndrome

8q13 microdeletion syndrome · Del(8)q(13)

ORPHA:2496

Mitochondrial DNA depletion syndrome

mtDNA depletion syndrome

ORPHA:35698

Monosomy 18q syndrome

18q- syndrome · Deletion 18q

ORPHA:1600

Monosomy 9p syndrome

9p deletion syndrome · 9p- syndrome

ORPHA:261112

Multiple mitochondrial DNA deletion syndrome

Multiple mtDNA deletion syndrome

ORPHA:254807

Non-distal deletion 10q syndrome

Non-distal monosomy 10q · Non-telomeric monosomy 10q

ORPHA:1581

Non-distal deletion 12q syndrome

Non-distal monosomy 12q · Non-telomeric monosomy 12q

ORPHA:96160

Partial autosomal deletion syndrome

Partial autosomal monosomy

ORPHA:98142

Partial deletion of chromosome 1 syndrome

Partial monosomy of chromosome 1

ORPHA:261766

Partial deletion of chromosome 10 syndrome

Partial monosomy of chromosome 10

ORPHA:261811

Partial deletion of chromosome 11 syndrome

Partial monosomy of chromosome 11

ORPHA:261816

Partial deletion of chromosome 12 syndrome

Partial monosomy of chromosome 12

ORPHA:282124

Partial deletion of chromosome 16 syndrome

Partial monosomy of chromosome 16

ORPHA:261826

Partial deletion of chromosome 17 syndrome

Partial monosomy of chromosome 17

ORPHA:261831

Partial deletion of chromosome 18 syndrome

Partial monosomy of chromosome 18

ORPHA:261836

Partial deletion of chromosome 19 syndrome

Partial monosomy of chromosome 19

ORPHA:261841

Partial deletion of chromosome 2 syndrome

Partial monosomy of chromosome 2

ORPHA:261771

Partial deletion of chromosome 20 syndrome

Partial monosomy of chromosome 20

ORPHA:261846

Partial deletion of chromosome 3 syndrome

Partial monosomy of chromosome 3

ORPHA:261776

Partial deletion of chromosome 4 syndrome

Partial monosomy of chromosome 4

ORPHA:261781

Partial deletion of chromosome 5 syndrome

Partial monosomy of chromosome 5

ORPHA:261786

Partial deletion of chromosome 6 syndrome

Partial monosomy of chromosome 6

ORPHA:261791

Partial deletion of chromosome 7 syndrome

Partial monosomy of chromosome 7

ORPHA:261796

Partial deletion of chromosome 8 syndrome

Partial monosomy of chromosome 8

ORPHA:261801

Partial deletion of chromosome 9 syndrome

Partial monosomy of chromosome 9

ORPHA:261806

Partial deletion of chromosome X syndrome

Partial monosomy of chromosome X

ORPHA:263726

Partial deletion of the long arm of chromosome 11 syndrome

Partial deletion of chromosome 11q · Partial monosomy of chromosome 11q

ORPHA:262092

Partial deletion of the short arm of chromosome 11 syndrome

Partial deletion of chromosome 11p · Partial monosomy of chromosome 11p

ORPHA:261947

Paternal 20q13.2q13.3 microdeletion syndrome

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

ORPHA:261304

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

Prader-Willi syndrome due to paternal 15q11q13 deletion

ORPHA:98793

SATB2-associated syndrome due to a chromosomal rearrangement

Del(2)(q33.1) · Monosomy 2q33.1

ORPHA:251028

Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion

5q31.3 microdeletion syndrome · Del(5)(q31.3)

ORPHA:314655

Smith-Magenis syndrome

17p11.2 microdeletion syndrome

ORPHA:819

Temple syndrome due to paternal 14q32.2 microdeletion

Paternal del(14)(q32.2)

ORPHA:254525

X-linked Alport syndrome-diffuse leiomyomatosis

Xq22.3 microdeletion syndrome

ORPHA:1018

Xp21 deletion syndrome

Del(X)(p21) · Xp21 contiguous gene deletion syndrome

ORPHA:261476

Xp22.3 microdeletion syndrome

Del(X)(p23)

ORPHA:1643