Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Idiopathic growth hormone deficiency |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Growth hormone neurosecretory dysfunction |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Psychosocial growth hormone deficiency |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Isolated somatotropin deficiency |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Transient somatotropin deficiency |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Pituitary dwarfism |
Is a |
False |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Adult growth hormone deficiency (disorder) |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Growth hormone deficiency after bone marrow transplant (disorder) |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Partial growth hormone deficiency |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
Growth delay due to insulin-like growth factor I deficiency is characterized by the association of intrauterine and postnatal growth retardation with sensorineural deafness and intellectual deficit. |
Is a |
False |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|
A multiple congenital anomalies syndrome characterized by wormian bones, dextrocardia and short stature due to a growth hormone deficiency. Additional manifestations that have been reported include brachycamptodactyly, kidney hypoplasia, bilateral cryptorchidism, midshaft hypospadias, imperforate anus/anorectal agenesis, body asymmetry, mild developmental delay, hemimegalencephaly and facial dysmorphism (hypotelorism, downslanting palpebral fissures, low-set and posteriorly angulated ears, depressed nasal bridge, and microstomia). |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Autosomal recessive isolated somatotropin deficiency |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Pituitary dwarfism with large sella turcica |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Pituitary dwarfism |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Ateleiotic dwarfism |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Pituitary dwarfism with normal somatotropin level AND low somatomedin |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Pituitary dwarfism with small sella turcica |
Due to |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
2 |
Hereditary growth hormone deficiency (disorder) |
Is a |
True |
Growth hormone deficiency (disorder) |
Inferred relationship |
Some |
|