Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the POU1F1 gene.
Comprehensive, easy-to-understand information about this condition
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isolated congenital growth hormone deficiency
MONDO:0000050
septooptic dysplasia
MONDO:0008428
congenital isolated adrenocorticotropic hormone deficiency
MONDO:0008720
non-acquired combined pituitary hormone deficiency with spine abnormalities
MONDO:0009091
short stature-pituitary and cerebellar defects-small sella turcica syndrome
MONDO:0009880
pituitary hormone deficiency, combined, 6
MONDO:0013518