|
infantile systemic hyalinosis
|
16331 |
|
|
corneal dystrophy, hereditary
|
D003317 |
|
|
obsolete hemiplegic migraine
|
23310.0 |
|
|
congenital, with hyperextensibility of fingers and facial dysmorphism dislocation of hip
|
C563315 |
|
|
congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
|
13310 |
|
|
congenital adrenal hyperplasia due to cytochrome POR deficiency
|
13310 |
|
|
gingival, with hypertrichosis and mental retardation fibromatosis
|
C565331 |
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, NK cell-positive
|
C563311 |
|
|
cancer of large intestine
|
24331 |
|
|
carcinoma of large intestine
|
24331 |
|
