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 ×

Krabbe disease

GALC deficiency · Galactocerebrosidase deficiency

ORPHA:487

Acatalasemia

Catalase deficiency

ORPHA:926

Alpha-N-acetylgalactosaminidase deficiency

NAGA deficiency · Schindler disease

ORPHA:3137

B4GALT1-CDG

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

ORPHA:79332

Beta-mannosidosis

Beta-mannosidase deficiency

ORPHA:118

Biotinidase deficiency

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

ORPHA:79241

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

Farber disease

Acid ceramidase deficiency · Farber lipogranulomatosis

ORPHA:333

Fructose-1,6-bisphosphatase deficiency

FBPase deficiency · Fructose-1,6-diphosphatase deficiency

ORPHA:348

Fucosidosis

Alpha-L-fucosidase deficiency

ORPHA:349

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

Gaucher disease

Acid beta-glucosidase deficiency · Glucocerebrosidase deficiency

ORPHA:355

Generalized galactose epimerase deficiency

Generalized GALE deficiency · Generalized GALE-D

ORPHA:308487

Glycogen storage disease due to acid maltase deficiency

Alpha-1,4-glucosidase acid deficiency · GSD due to acid maltase deficiency

ORPHA:365

Glycogen storage disease due to glycogen debranching enzyme deficiency

GSDIII · Glycogen storage disease type 3

ORPHA:366

GM1 gangliosidosis

Beta-galactosidase-1 deficiency · GLB1 deficiency

ORPHA:354

Guanidinoacetate methyltransferase deficiency

GAMT deficiency

ORPHA:382

Histidinemia

HAL deficiency · HIS deficiency

ORPHA:2157

Hyaluronidase deficiency

MPS9 · MPSIX

ORPHA:67041

MOGS-CDG

CDG syndrome type IIb · CDG-IIb

ORPHA:79330

Mucopolysaccharidosis type 4A

GALNS deficiency · Galactosamine-6-sulfatase deficiency

ORPHA:309297

Mucopolysaccharidosis type 4B

Beta-D-galactosidase deficiency · MPS4B

ORPHA:309310

Prolidase deficiency

Hyperimidodipeptiduria

ORPHA:742

Purine nucleoside phosphorylase deficiency

PNP deficiency · PNPase deficiency

ORPHA:760

Trehalase deficiency

Isolated trehalose intolerance

ORPHA:103909