|
lymphoproliferative syndrome, ebv-associated, autosomal, 1
|
C567815 |
|
|
autosomal dominant emery-dreifuss muscular dystrophy 4
|
C567831 |
|
|
vascular malformations, epidermal nevi, and skeletal-spinal abnormalities congenital lipomatous overgrowth
|
C567863 |
|
|
7 generalized epilepsy with febrile seizures plus
|
C567827 |
|
|
febrile convulsions, familial, 3a
|
C567820 |
|
|
febrile convulsions, familial, 3b
|
C567821 |
|
|
familial, 3b febrile convulsions
|
C567821 |
|
|
familial, 3a febrile convulsions
|
C567820 |
|
|
convulsions, familial febrile, 3a
|
C567820 |
|
|
seizures, familial febrile, 3a
|
C567820 |
|
|
type 7 generalized epilepsy with febrile seizures plus
|
C567827 |
|
|
dysplasia of head of femur, Meyer type
|
15678 |
|
|
global cerebral hypomyelination
|
C567847 |
|
|
emmonsia crescens infection
|
C000656784 |
|
|
basidiobolus ranarum infection
|
C000656785 |
|
