|
spinocerebellar atrophy IIIs
|
D017827 |
|
|
immunodeficiency 18; IMD18
|
http://purl.obolibrary.org/obo/MONDO_0014278 |
|
|
HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES
|
32780 |
|
|
autosomal dominant KID syndrome
|
7850 |
|
|
hyperpyrexia, malignant;MH KING syndrome, included
|
7783 |
|
|
Kearns-Sayre syndrome; KSS
|
http://purl.obolibrary.org/obo/MONDO_0010787 |
|
|
autosomal dominant Kenny-Caffey syndrome
|
7478 |
|
|
LACRIMOAURICULODENTODIGITAL syndrome; LADD
|
http://purl.obolibrary.org/obo/MONDO_0007872 |
|
|
Lamb-Shaffer syndrome; LAMSHF
|
14778 |
|