|
von willebrand disease, type IIN
|
D056728 |
|
|
von willebrand disease, type i
|
D056725 |
|
|
deafness, autosomal dominant, due to mutation in Myo1a
|
C567266 |
|
|
epidermolysis bullosa dystrophica with subcorneal cleavage
|
C567272 |
|
|
deafness, autosomal dominant 3a
|
C567277 |
|
|
deafness, autosomal dominant 3b
|
C567215 |
|
|
febrile convulsions, familial, 10
|
C567218 |
|
|
autosomal dominant, due to mutation in Myo1a deafness
|
C567266 |
|
|
familial, 10 febrile convulsions
|
C567218 |
|
|
seizures, familial febrile, 10
|
C567218 |
|
|
autosomal dominant hypercarotenemia and vitamin a deficiency
|
C567296 |
|
|
amelogenesis imperfecta, hypomaturation type, iia2
|
C567279 |
|
|
1q21.1 contiguous gene deletion
|
C567291 |
|
|
mental retardation, joint hypermobility, and skin laxity, with or without metabolic abnormalities
|
C567209 |
|
