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"

17 matching diseasesClear search ×

Mucopolysaccharidosis type 4A

GALNS deficiency · Galactosamine-6-sulfatase deficiency

ORPHA:309297

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

DPAGT1-CDG

CDG syndrome type Ij · CDG-Ij

ORPHA:86309

Metachromatic leukodystrophy

Arylsulfatase A deficiency · MLD

ORPHA:512

MGAT2-CDG

CDG syndrome type IIa · CDG-IIa

ORPHA:79329

Mucolipidosis type II

I-cell disease · N-acetylglucosamine 1-phosphotransferase deficiency

ORPHA:576

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 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 B

MPS3B · MPSIIIB

ORPHA:79270

Sanfilippo syndrome type D

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

ORPHA:79272