|
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10
|
32777 |
|
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES
|
32779 |
|
|
NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT
|
32775 |
|
|
arthrogryposis multiplex congenita, myogenic type
|
32778 |
|
|
papillary thyroid microcarcinoma
|
C563277 |
|
|
intellectual developmental disorder with severe speech and ambulation defects
|
32770 |
|
|
early infantile epileptic encephalopathy caused by mutation in SPTAN1
|
13277 |
|
|
developmental and epileptic encephalopathy, 5
|
13277 |
|
|
cerebellar, ocular, craniofacial, and genital syndrome
|
32774 |
|
|
SPTAN1 early infantile epileptic encephalopathy
|
13277 |
|
|
epileptic encephalopathy, early infantile, 5
|
13277 |
|
|
epileptic encephalopathy, early infantile, 5; EIEE5
|
http://purl.obolibrary.org/obo/MONDO_0013277 |
|
|
epileptic encephalopathy, early infantile, type 5
|
13277 |
|
