Human (60 sources):
Abdominal distention,
Abnormal digit morphology,
Abnormal prolactin level,
Abnormality of secondary sexual hair,
Abnormality of the face,
Abnormality of the hypothalamus-pituitary axis,
Abnormality of the orbital region,
Absence of secondary sex characteristics,
Absent septum pellucidum,
Adrenal insufficiency,
Agenesis of corpus callosum,
Amenorrhea,
Anterior pituitary agenesis,
Anterior pituitary hypoplasia,
Aplasia/Hypoplasia of the breasts,
Central hypothyroidism,
Coarse facial features,
Constipation,
Decreased cervical spine mobility,
Decreased circulating ACTH level,
Decreased response to growth hormone stimulation test,
Decreased testicular size,
Delayed puberty,
Delayed skeletal maturation,
Depressed nasal ridge,
Ectopic anterior pituitary gland,
Ectopic posterior pituitary,
Fatigue,
Feeding difficulties,
Global developmental delay,
Growth delay,
Holoprosencephaly,
Hypoglycemia,
Hypoglycemic seizures,
Hypogonadism,
Hypogonadotropic hypogonadism,
Hypopituitarism,
Hypotension,
Hypothyroidism,
Hypotonia,
Infertility,
Intellectual disability,
Jaundice,
Large fontanelles,
Median cleft lip and palate,
Neonatal hypoglycemia,
Optic nerve hypoplasia,
Orofacial cleft,
Osteopenia,
Osteoporosis of vertebrae,
Panhypopituitarism,
Pituitary dwarfism,
Pituitary hypothyroidism,
Polydactyly,
Seizure,
Septo-optic dysplasia,
Severe global developmental delay,
Short stature,
Sleep disturbance,
Umbilical hernia
[+]
|
These phenotypes are associated with this gene with a has phenotype relation via Monarch.