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"

9 matching diseasesClear search ×

Hyperkalemic periodic paralysis

Adynamia episodica hereditaria · Familial hyperPP

ORPHA:682

Familial pseudohyperkalemia

ORPHA:90044

Familial pseudohyperkalemia type 1

ORPHA:100039

Genetic periodic paralysis

ORPHA:371433

Hypokalemic periodic paralysis

Westphall disease

ORPHA:681

Normokalemic periodic paralysis

NormoKPP · NormoPP

ORPHA:680

Periodic paralysis

ORPHA:206976

Pseudohypoaldosteronism type 2

Chloride shunt syndrome · Familial hyperkalemic hypertension

ORPHA:757

Thyrotoxic periodic paralysis

Thyrotoxic hypokalemic periodic paralysis

ORPHA:79102