|
complex congenital heart defect, renal agenesis, and cleft lip and palate
|
C535327 |
|
|
intracranial cavernous hemangioma
|
2327 |
|
|
Hutchinson's melanotic freckle
|
D018327 |
|
|
hutchinson melanotic freckle
|
D018327 |
|
|
hutchinsons melanotic freckle
|
D018327 |
|
|
neuronal intranuclear hyaline inclusion disease
|
11327 |
|
|
HOGA1 primary hyperoxaluria
|
13327 |
|
|
facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome
|
32714 |
|
|
hyper-ige recurrent infection syndrome 4, autosomal recessive
|
32796 |
|
|
encephalopathy, acute, infection-induced, susceptibility to, 9
|
32742 |
|
|
spondyloepiphyseal dysplasia, kondo-fu type
|
32721 |
|
|
neuronal intranuclear inclusion disease
|
11327 |
|
|
SPTAN1 early infantile epileptic encephalopathy
|
13277 |
|
