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"

23 matching diseasesClear search ×

Tay-Sachs disease, infantile form

Beta-hexosaminidase subunit alpha deficiency, infantile form · GM2 gangliosidosis, Tay-Sachs variant, infantile form

ORPHA:309178

Free sialic acid storage disease, infantile form

ISSD

ORPHA:309324

Gaucher disease type 2

Acute neuronopathic Gaucher disease · Infantile cerebral Gaucher disease

ORPHA:77260

Glycogen storage disease due to acid maltase deficiency, infantile onset

Glycogenosis type II, infantile onset · Glycogen storage disease type II, infantile onset

ORPHA:308552

HSD10 disease, infantile type

2-methyl-3-hydroxybutyric aciduria, classic type · 2-methyl-3-hydroxybutyric aciduria, infantile type

ORPHA:391428

Infantile CLN1 disease

Infantile neuronal ceroid lipofuscinosis type 1

ORPHA:699718

Infantile CLN2 disease

Infantile neuronal ceroid lipofuscinosis type 2

ORPHA:699751

Infantile hypophosphatasia

Infantile phosphoethanolaminuria · Infantile Rathbun disease

ORPHA:247651

Infantile Krabbe disease

Krabbe disease, classic form · Krabbe disease, early-onset

ORPHA:206436

Infantile Refsum disease

IRD · Mild peroxisome biogenesis disorder-Zellweger spectrum disorder

ORPHA:772

Late infantile CLN1 disease

Late infantile neuronal ceroid lipofuscinosis type 1

ORPHA:699734

Late infantile CLN10 disease

Late infantile neuronal ceroid lipofuscinosis type 10

ORPHA:700492

Late infantile CLN2 disease

Infantile neuronal ceroid lipofuscinosis type 2

ORPHA:699761

Late infantile CLN5 disease

Late infantile neuronal ceroid lipofuscinosis type 5

ORPHA:699802

Late infantile CLN6 disease

Late infantile neuronal ceroid lipofuscinosis type 6

ORPHA:700467

Late infantile CLN8 disease

Late infantile neuronal ceroid lipofuscinosis type 8

ORPHA:700484

Late-infantile/juvenile Krabbe disease

Krabbe disease, late-onset

ORPHA:206443

OBSOLETE: Tay-Sachs disease, B1 variant

OBSOLETE: GM2 gangliosidosis, B1 variant · OBSOLETE: Hexosaminidase A deficiency, B1 variant

ORPHA:309239

Sandhoff disease, infantile form

GM2 gangliosidosis, Sandhoff variant, infantile form · GM2 gangliosidosis, hexosaminidase A and B deficiency variant, infantile form

ORPHA:309155

Severe Canavan disease

Infantile Canavan disease · Neonatal Canavan disease

ORPHA:314911

Tay-Sachs disease

Beta-hexosaminidase subunit alpha deficiency · GM2 gangliosidosis, Tay-Sachs variant

ORPHA:845

Tay-Sachs disease, adult form

GM2 gangliosidosis, Tay-Sachs variant, adult form · GM2 gangliosidosis, hexosaminidase A deficiency variant, adult form

ORPHA:309192

Tay-Sachs disease, juvenile form

Beta-hexosaminidase subunit alpha deficiency, juvenile form · GM2 gangliosidosis, Tay-Sachs variant, juvenile form

ORPHA:309185