|
pelger huet nuclear anomaly
|
D010381 |
|
|
pelger huët nuclear anomaly
|
D010381 |
|
|
pseudo pelger-huet nuclear anomaly
|
D010381 |
|
|
zonular central nuclear cataract
|
C565135 |
|
|
autosomal dominant nuclear cataract
|
C565137 |
|
|
cataract, congenital, nuclear progressive
|
C564596 |
|
|
cataract, congenital nuclear, autosomal recessive 1
|
C563728 |
|
|
cataract, congenital nuclear, autosomal recessive 2
|
C565725 |
|
|
cataract, congenital nuclear, autosomal recessive 3
|
C566923 |
|
|
atpase deficiency, nuclear-encoded
|
C564021 |
|
|
hypersegmentation of nuclei of polymorphonuclear leukocytes
|
C566014 |
|
|
ovoid neutrophil nuclei, developmental delay, epilepsy and skeletal abnormalities
|
D010381 |
|
|
ovoid neutrophil nuclei, developmental delay, epilepsy, and skeletal abnormalities
|
D010381 |
|
|
pyrimidine 5-prime nucleotidase deficiency, hemolytic anemia due to
|
C564859 |
|
