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"

140 matching diseasesClear search ×

Farber disease

Acid ceramidase deficiency · Farber lipogranulomatosis

ORPHA:333

3-hydroxy-3-methylglutaric aciduria

3-hydroxy-3-methylglutaryl-CoA lyase deficiency · HMG-CoA lyase deficiency

ORPHA:20

3-methylcrotonyl-CoA carboxylase deficiency

3-methylcrotonylglycinuria · MCC deficiency

ORPHA:6

Acatalasemia

Catalase deficiency

ORPHA:926

Acid sphingomyelinase deficiency

ASMD

ORPHA:618899

Acquired hemophilia A

Acquired factor VIII deficiency · Acquired F8 deficiency

ORPHA:599480

Acquired hemophilia B

Acquired factor IX deficiency · Acquired F9 deficiency

ORPHA:599485

Acyl-CoA dehydrogenase 9 deficiency

ACAD9 deficiency

ORPHA:99901

Acyl-CoA dehydrogenase deficiency

ORPHA:309120

Adenine phosphoribosyltransferase deficiency

2,8-dihydroxyadenine urolithiasis · APRT deficiency

ORPHA:976

Adenosine monophosphate deaminase deficiency

AMP deaminase deficiency · Myoadenylate deaminase deficiency

ORPHA:45

Adenylosuccinate lyase deficiency

ADSL deficiency · Adenylosuccinase deficiency

ORPHA:46

AICA-ribosiduria

5-amino-4-imidazole carboxamide ribosiduria · ATIC deficiency

ORPHA:250977

Alkaline ceramidase 3 deficiency

Leukodystrophy due to alkaline ceramidase 3 deficiency · ACER3-related early childhood-onset progressive leukodystrophy

ORPHA:502444

Alkaptonuria

Hereditary ochronosis · Homogentisic acid oxidase deficiency

ORPHA:56

Alpha-N-acetylgalactosaminidase deficiency

NAGA deficiency · Schindler disease

ORPHA:3137

Aminoacylase 1 deficiency

ACY1D · N-acyl-L-amino acid amidohydrolase deficiency

ORPHA:137754

Aminoacylase deficiency

ORPHA:308448

Apolipoprotein A-I deficiency

ApoA-I deficiency · Familial apoA-I deficiency

ORPHA:425

Argininemia

Arginase 1 deficiency · Arginase deficiency

ORPHA:90

Argininosuccinic aciduria

ASA deficiency · ASL deficiency

ORPHA:23

Aromatase deficiency

Congenital estrogen deficiency

ORPHA:91

Aromatic L-amino acid decarboxylase deficiency

AADC deficiency

ORPHA:35708

Aspartylglucosaminuria

Aspartylglucosaminidase deficiency

ORPHA:93

Autosomal dominant combined immunodeficiency due to ERBIN deficiency

AD-CID due to ERBIN deficiency · Autosomal dominant combined immunodeficiency due to erbb2 interacting protein deficiency

ORPHA:656912

Autosomal recessive combined immunodeficiency due to IL6R deficiency

AR CID due to IL6R deficiency · Autosomal recessive combined immunodeficiency due to IL6 receptor protein deficiency

ORPHA:656326

Autosomal recessive extra-oral halitosis

Methanethiol oxidase deficiency · MTO-deficiency

ORPHA:562538

Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity

Autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity · CD16 deficiency

ORPHA:437552

Beta-ketothiolase deficiency

3-ketothiolase deficiency · 3-oxothiolase deficiency

ORPHA:134

Beta-mannosidosis

Beta-mannosidase deficiency

ORPHA:118

Bile acid CoA ligase deficiency and defective amidation

ORPHA:276066

Biotinidase deficiency

Juvenile-onset multiple carboxylase deficiency · Late-onset multiple carboxylase deficiency

ORPHA:79241

Canavan disease

ACY2 deficiency · Aminoacylase 2 deficiency

ORPHA:141

Carbamoyl-phosphate synthetase 1 deficiency

CPS1 deficiency · CPS1D

ORPHA:147

Carnitine palmitoyl transferase 1A deficiency

CPT1A deficiency · Carnitine palmitoyl transferase IA deficiency

ORPHA:156

Carnitine-acylcarnitine translocase deficiency

CACT deficiency

ORPHA:159

Carnosinase deficiency

ORPHA:1361

Cernunnos-XLF deficiency

Cernunnos XLFD · Cernunnos deficiency

ORPHA:169079

Chronic visceral acid sphingomyelinase deficiency

Chronic visceral ASMD · Niemann-Pick disease type B

ORPHA:77293

Citrin deficiency

ORPHA:247582

Citrullinemia type I

ASS deficiency · Argininosuccinate synthase deficiency

ORPHA:247525

Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome

Hyaluronidase 2 deficiency · Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-deafness syndrome

ORPHA:508476

Coenzyme Q10 deficiency

Primary coenzyme Q10 deficiency · CoQ10 deficiency

ORPHA:35656

Combined immunodeficiency due to c-REL deficiency

CID due to c-REL deficiency · Combined immunodeficiency due to cellular homolog of v-Rel deficiency

ORPHA:697394

Combined immunodeficiency due to CARD11 deficiency

CID due to CARD11 deficiency · Combined immunodeficiency due to caspase recruitment domain family member 11 protein deficiency

ORPHA:357237

Combined immunodeficiency due to CD27 deficiency

CD27 deficiency · Autosomal recessive lymphoproliferative disease due to CD27 deficiency

ORPHA:238505

Combined immunodeficiency due to DOCK2 deficiency

Combined immunodeficiency due to dedicator of cytokinesis 2 protein deficiency · CID due to DOCK2 deficiency

ORPHA:447737

Combined immunodeficiency due to DOCK8 deficiency

CID due to DOCK8 deficiency · Combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency

ORPHA:217390