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"

53 matching diseasesClear search ×

Disorder of gamma-aminobutyric acid metabolism

Disorder of GABA metabolism

ORPHA:79175

Disorder of amino acid and other organic acid metabolism

ORPHA:79062

Disorder of asparagine metabolism

ORPHA:391381

Disorder of beta and omega amino acid metabolism

ORPHA:308407

Disorder of bilirubin metabolism and excretion

ORPHA:309816

Disorder of biogenic amine metabolism and transport

ORPHA:79214

Disorder of branched-chain amino acid metabolism

ORPHA:79197

Disorder of carbohydrate metabolism

ORPHA:79161

Disorder of cobalamin metabolism and transport

ORPHA:79171

Disorder of copper metabolism

ORPHA:309839

Disorder of energy metabolism

ORPHA:79200

Disorder of fatty acid oxidation and ketone body metabolism

ORPHA:79174

Disorder of folate metabolism and transport

ORPHA:285657

Disorder of fructose metabolism

ORPHA:308463

Disorder of galactose metabolism

ORPHA:308467

Disorder of glutamine metabolism

ORPHA:289841

Disorder of glycerol metabolism

ORPHA:79179

Disorder of glyoxylate metabolism

ORPHA:308998

Disorder of histidine metabolism

ORPHA:79181

Disorder of iron metabolism and transport

ORPHA:309842

Disorder of lipid metabolism

ORPHA:309005

Disorder of lysine and hydroxylysine metabolism

ORPHA:289832

Disorder of melanin metabolism

ORPHA:352728

Disorder of metabolite absorption and transport

ORPHA:309824

Disorder of methionine cycle and sulfur amino acid metabolism

Cytosolic methyl group transfer or sulfur amino acid metabolism disorder

ORPHA:79173

Disorder of neurotransmitter metabolism and transport

ORPHA:79169

Disorder of ornithine metabolism

ORPHA:289869

Disorder of ornithine or proline metabolism

ORPHA:79185

Disorder of other vitamins and cofactors metabolism and transport

ORPHA:309833

Disorder of pentose phosphate metabolism

ORPHA:79186

Disorder of peptide metabolism

ORPHA:79187

Disorder of phenylalanin or tyrosine metabolism

ORPHA:79190

Disorder of phenylalanine metabolism

ORPHA:284814

Disorder of porphyrin and heme metabolism

ORPHA:309813

Disorder of proline metabolism

ORPHA:289866

Disorder of pterin metabolism

ORPHA:309819

Disorder of purine metabolism

ORPHA:79191

Disorder of purine or pyrimidine metabolism

ORPHA:79224

Disorder of pyridoxine metabolism

ORPHA:79192

Disorder of pyrimidine metabolism

ORPHA:79193

Disorder of serine or glycine metabolism

ORPHA:79194

Disorder of sialic acid metabolism

ORPHA:309319

Disorder of thiamine metabolism and transport

ORPHA:298644

Disorder of tryptophan metabolism

ORPHA:289829

Disorder of tyrosine metabolism

ORPHA:284818

Disorder of urea cycle metabolism and ammonia detoxification

ORPHA:79167

Disorder of zinc metabolism and transport

ORPHA:309845

Disorders of pentose/polyol metabolism

ORPHA:440701