Parent term(s)
Term with siblings
atransferrinemia
autosomal dominant hypocalcemia +
familial periodic paralysis +
hemochromatosis +
hypermanganesemia with dystonia +
Menkes disease
molybdenum cofactor deficiency +
occipital horn syndrome
primary hypomagnesemia +
pseudohypoparathyroidism +
Wilson disease
acrodermatitis enteropathica
atransferrinemia
autosomal dominant hypocalcemia +
familial periodic paralysis +
hemochromatosis +
hypermanganesemia with dystonia +
Menkes disease
molybdenum cofactor deficiency +
occipital horn syndrome
primary hypomagnesemia +
pseudohypoparathyroidism +
Wilson disease
Child term(s)
denotes an 'is-a' relationship