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 ×

Mucopolysaccharidosis type 4A

GALNS deficiency · Galactosamine-6-sulfatase deficiency

ORPHA:309297

Acatalasemia

Catalase deficiency

ORPHA:926

Alpha-N-acetylgalactosaminidase deficiency

NAGA deficiency · Schindler disease

ORPHA:3137

Alpha-N-acetylgalactosaminidase deficiency type 1

NAGA deficiency type 1 · Schindler disease type 1

ORPHA:79279

Alpha-N-acetylgalactosaminidase deficiency type 2

Adult-onset Alpha-N-acetylgalactosaminidase deficiency · Kanzaki disease

ORPHA:79280

Alpha-N-acetylgalactosaminidase deficiency type 3

NAGA deficiency type 3 · Schindler disease type 3

ORPHA:79281

B4GALT1-CDG

Beta-1,4-galactosyltransferase deficiency · CDG syndrome type IId

ORPHA:79332

Classic galactosemia

GALT deficiency · Galactose-1-phosphate uridyltransferase deficiency

ORPHA:79239

Erythrocyte galactose epimerase deficiency

Erythrocyte GALE deficiency · Erythrocyte GALE-D

ORPHA:308473

Fabry disease

Alpha-galactosidase A deficiency · Anderson-Fabry disease

ORPHA:324

Fructose-1,6-bisphosphatase deficiency

FBPase deficiency · Fructose-1,6-diphosphatase deficiency

ORPHA:348

Galactokinase deficiency

GALK deficiency · GALK-D

ORPHA:79237

Galactose epimerase deficiency

Epimerase deficiency galactosemia · GALE deficiency

ORPHA:79238

Galactosialidosis

Goldberg syndrome · Neuraminidase deficiency with beta-galactosidase deficiency

ORPHA:351

Gamma-aminobutyric acid transaminase deficiency

GABA transaminase deficiency

ORPHA:2066

Generalized galactose epimerase deficiency

Generalized GALE deficiency · Generalized GALE-D

ORPHA:308487

GM1 gangliosidosis

Beta-galactosidase-1 deficiency · GLB1 deficiency

ORPHA:354

Krabbe disease

GALC deficiency · Galactocerebrosidase deficiency

ORPHA:487

Metachromatic leukodystrophy

Arylsulfatase A deficiency · MLD

ORPHA:512

Metachromatic leukodystrophy, adult form

Arylsulfatase A deficiency, adult form · MLD, adult form

ORPHA:309271

Mucopolysaccharidosis type 2

Hunter syndrome · Iduronate 2-sulfatase deficiency

ORPHA:580

Mucopolysaccharidosis type 2, attenuated form

Hunter syndrome type B · Iduronate 2-sulfatase deficiency type B

ORPHA:217093

Mucopolysaccharidosis type 2, severe form

Hunter syndrome type A · Iduronate 2-sulfatase deficiency type A

ORPHA:217085

Mucopolysaccharidosis type 4B

Beta-D-galactosidase deficiency · MPS4B

ORPHA:309310

Mucopolysaccharidosis type 6

ARSB deficiency · ASB deficiency

ORPHA:583

Multiple sulfatase deficiency

MSD · Austin disease

ORPHA:585

Recessive X-linked ichthyosis

RXLI · Steroid sulfatase deficiency

ORPHA:461

Sanfilippo syndrome type A

Mucopolysaccharidosis type IIIA · Heparan sulfamidase deficiency

ORPHA:79269

Sanfilippo syndrome type D

GNS deficiency · Glucosamine N-acetyl-6-sulfatase deficiency

ORPHA:79272