|
maternal disease-related embryofetopathy
|
16678 |
|
|
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 |
|
|
developmental and epileptic encephalopathy, 71
|
32678 |
|
|
rare inborn error of pyruvate metabolic process
|
16789 |
|
|
juvenile spring eruption of ears
|
C566781 |
|
|
polymorphic light eruption, hereditary
|
C566780 |
|
|
febrile convulsions, familial, 3a
|
C567820 |
|
|
febrile convulsions, familial, 3b
|
C567821 |
|
|
atrial fibrillation, familial, 5
|
12678 |
|
|
atrial fibrillation, familial, 5; ATFB5
|
http://purl.obolibrary.org/obo/MONDO_0012678 |
|
|
familial, 3b febrile convulsions
|
C567821 |
|
|
familial, 3a febrile convulsions
|
C567820 |
|
|
convulsions, familial febrile, 3a
|
C567820 |
|
