|
chromosome abnormality disorder
|
19040 |
|
|
chromosome Abnormality disorder
|
http://purl.obolibrary.org/obo/MONDO_0019040 |
|
|
autosomal chromosome disorders
|
19040 |
|
|
chromosome abnormality disorders
|
19040 |
|
|
chromosome Abnormality disorders
|
http://purl.obolibrary.org/obo/MONDO_0019040 |
|
|
SCN2A benign familial infantile epilepsy
|
11904 |
|
|
convulsions, benign familial infantile, 3
|
11904 |
|
|
seizures, benign familial neonatal-infantile
|
11904 |
|
|
seizures, benign familial infantile, 3
|
11904 |
|
|
seizures, benign familial infantile, 3; BFIS3
|
http://purl.obolibrary.org/obo/MONDO_0011904 |
|
|
seizures, benign familial infantile, type 3
|
11904 |
|
|
tumor of hematopoietic and lymphoid tissues
|
19044 |
|
|
obsolete rare genetic inherited tumor
|
19041.0 |
|
|
obsolete rare genetic skin disease
|
19043.0 |
|
