|
CEREBROCOSTOMANDIBULAR syndrome
|
7301 |
|
|
cerebro-costo-mandibular syndrome
|
7301 |
|
|
cerebrocostomandibular syndrome
|
7301 |
|
|
griscelli syndrome, cutaneous and neurologic type
|
C537301 |
|
|
CEREBROCOSTOMANDIBULAR syndrome; CCMS
|
http://purl.obolibrary.org/obo/MONDO_0007301 |
|
|
lactic acidosis, congenital infantile, due to LAD deficiency
|
C573012 |
|
|
type III maple syrup urine disease
|
C573012 |
|
|
pericardial and diaphragmatic defect
|
17301 |
|
|
rib Gap defects with micrognathia
|
7301 |
|
|
congenital infantile, due to LAD deficiency lactic acidosis
|
C573012 |
|
|
lactic acidosis due to lipoamide dehydrogenase deficiency
|
C573012 |
|
|
type 1 griscelli syndrome
|
C537301 |
|
|
griscelli syndrome type 1
|
C537301 |
|
