Rare Disease Intelligence

Migraine disorder is a common vascular headache characterized by recurrent, severe head pain often accompanied by symptoms such as nausea, vomiting, a...

Familial hemiplegic migraine type 1 is a neurological condition that is classified as a severe variant of migraine with aura, characterized by transie...

Migraine, familial hemiplegic, 2 is a neurological condition caused by mutations in the ATP1A2 gene. It is characterized by severe migraine headaches...

Migraine, familial hemiplegic, 3 is a neurological condition characterized by episodes of migraine with aura that may include motor weakness and alter...

Familial hemiplegic migraine, type 4 is a subtype of migraine characterized by episodes of severe headache that may be accompanied by temporary unilat...

Mild Canavan disease is a neurodegenerative condition that primarily affects brain development and motor skills. It is characterized by mild delays in...

Mild hemophilia A is a bleeding disorder characterized by a small deficiency of factor VIII, which can lead to abnormal bleeding after minor injuries,...

Mild hemophilia B is a bleeding disorder in which a small deficiency of clotting factor IX leads to abnormal bleeding after minor injuries or surgical...

Mild hyperphenylalaninemia is a rare metabolic disorder that represents a milder form of phenylketonuria, an inborn error of amino acid metabolism. It...