| hereditary ectodermal p. |
anhidrotic ectodermal dysplasia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| hereditary essential t. |
essential t.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hereditary f. of bone |
osteogenesis imperfecta.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hereditary fructose i. |
an autosomal recessive carbohydrate intolerance due to deficiency of fructose bisphosphate aldolase, isozyme B, with onset in infancy; it is characterized by hypoglycemia, with variable manifestations of fructosuria, fructosemia, anorexia, vomiting, failure to thrive, jaundice, splenomegaly, and an aversion to fructose-containing foods. If untreated, it may be fatal. See also essential fructosuria, under fructosuria.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hereditary h. of neutrophils |
a hereditary condition in which the neutrophils are multilobed; called also Undritz anomaly.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|