Hyperparathyroidism, transient neonatal is a condition observed in newborns that involves a temporary disruption in parathyroid hormone regulation. Th...

Hyperphenylalaninemia due to tetrahydrobiopterin deficiency is a rare inherited metabolic disorder in which the body cannot properly break down the am...

Hyperphosphatasia-intellectual disability syndrome, also known as HPMR or Mabry syndrome, is a condition that primarily affects neurodevelopment and c...

Hyperphosphatasia with intellectual disability syndrome 1 is a genetic condition that affects multiple systems, particularly the central nervous syste...

Hyperphosphatasia with intellectual disability syndrome 2 is an inherited multisystem condition primarily affecting neurodevelopment and skeletal form...

Hyperphosphatasia with intellectual disability syndrome 3 is a genetic condition caused by mutations in the PGAP2 gene that disrupt glycosylphosphatid...

Hyperphosphatasia with intellectual disability syndrome 4 is a genetic condition that primarily affects neurodevelopment and physical features. It is...

Hyperphosphatasia with intellectual disability syndrome 5 is a multisystem condition characterized by distinctive facial features, hernias, seizures,...

Hyperphosphatasia with intellectual disability syndrome 6 is a multi-system condition characterized by elevated alkaline phosphatase levels combined w...

Hyperprolinemia is a metabolic condition characterized by an elevated level of the amino acid proline in the blood. It results from a disruption in th...

Hypersensitivity pneumonitis is a lung condition characterized by inflammation due to an immune reaction following repeated exposure to inhaled organi...

Hypersensitivity pneumonitis, familial is an inherited form of lung inflammation that arises in individuals with a genetic predisposition to reacting...