|
male, with gynecomastia pseudohermaphroditism
|
C537805 |
|
|
teebi al-saleh hassoon syndrome
|
C537830 |
|
|
nonsyndromic hereditary hearing impairment
|
C537845 |
|
|
nonsyndromic sensorineural hearing loss
|
C537845 |
|
|
corneal dystrophy, hereditary polymorphous posterior
|
7378 |
|
|
fibromatosis gingival, hereditary, 3
|
12378 |
|
|
fibromatosis, gingival, hereditary, 3
|
12378 |
|
|
congenital nonautoimmune hyperthyroidism
|
C563786 |
|
|
methemoglobinemia, type i
|
C537841 |
|
|
distal, type i arthrogryposis multiplex congenita
|
C535378 |
|
|
lattice type i corneal dystrophy
|
C537881 |
|
|
familial, type i hyperreninemic hypoaldosteronism
|
C537806 |
|
|
methemoglobinemia, type ii
|
C537841 |
|
