Genetic Conditions - I

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Genetic Conditions…

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IAHSP see infantile-onset ascending hereditary spastic paralysis

idiopathic hemochromatosis see hemochromatosis, type 3

Idiopathic neonatal hemochromatosis see hemochromatosis, neonatal

Idiopathic pulmonary hypertension see primary pulmonary hypertension

Immune System and Disorders

incontinentia pigmenti

Infantile cerebral Gaucher's disease see Gaucher disease, type 2

Infantile Gaucher Disease see Gaucher disease, type 2

infantile-onset ascending hereditary spastic paralysis

inherited emphysema see alpha-1 antitrypsin deficiency

Inherited Human Transmissible Spongiform Encephalopathies see prion disease

inherited tendency to pressure palsies see hereditary neuropathy with liability to pressure palsies

Insley-Astley syndrome see otospondylomegaepiphyseal dysplasia

Intermittent acute porphyria syndrome see acute intermittent porphyria

Intestinal polyposis-cutaneous pigmentation syndrome see Peutz-Jeghers syndrome

IP see incontinentia pigmenti

Iron storage disorder see hemochromatosis

Isolated deafness see nonsyndromic deafness

isovaleric acidemia

Isovaleryl-CoA dehydrogenase deficiency see isovaleric acidemia

IVD deficiency see isovaleric acidemia