kallmann syndrome, type 1, X-linked
|
D017436 |
|
kallmann syndrome, type 3, recessive
|
D017436 |
|
anosmia, and midline cranial anomalies (cleft lip, cleft palate and imperfect fusion) hypogonadotropic hypogonadism
|
D017436 |
|
anosmic idiopathic hypogonadotropic hypogonadism
|
D017436 |
|
autosomal dominant form of kallmann syndrome
|
D017436 |
|
autosomal recessive form of kallmann syndrome
|
D017436 |
|
dysplasia olfactogenitalis of de morsier
|
D017436 |
|