Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Isolated gonadotropin deficiency |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Follicle stimulating hormone deficiency |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
LH - luteinising hormone deficiency |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Idiopathic hypogonadotropic hypogonadism |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Female hypogonadotropic hypogonadism |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Adiposogenital dystrophy (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Hypogonadism with anosmia |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism due to luteinizing hormone deficiency (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
This syndrome is characterized by the association of hypogonadotropic hypogonadism and frontoparietal alopecia. |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
A syndrome with the association of demyelinating leukodystrophy and progressive cerebellar ataxia, hypogonadotropic hypogonadism and hypodontia. It has been diagnosed in four unrelated patients. These symptoms suggest the association of a myelination defect (of the central and peripheral nervous systems) with an endocrinal deficiency of the pituitary gland. |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
This syndrome is characterized by the association of intellectual deficit, congenital cataract, and hypogonadotropic hypogonadism. |
Is a |
False |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Congenital hypogonadotropic hypogonadism (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Functional hypogonadotropic hypogonadism (disorder) |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
A very rare autosomal recessive, slowly progressive neurodegenerative disorder characterized by the triad of cerebellar ataxia (that generally manifests at adolescence or early adulthood), chorioretinal dystrophy, which may have a later onset (up to the fifth-sixth decade) leading to variable degrees of visual impairment, and hypogonadotropic hypogonadism (delayed puberty and lack of secondary sex characteristics). Ataxia-hypogonadism-choroidal dystrophy syndrome belongs to a clinical continuum of neurodegenerative disorders along with the clinically overlapping cerebellar ataxia-hypogonadism syndrome. |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
Progressive cerebellar ataxia with hypogonadism |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
A rare hypomyelinating leukodystrophy disorder characterized by the association of dental abnormalities (delayed dentition, abnormal order of dentition, hypodontia), hypogonadotropic hypogonadism, and hypomyelinating leukodystrophy manifesting with neurodevelopmental delay or regression and/or progressive cerebellar symptoms. |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|
A rare genetic disease characterized by childhood onset of multiple endocrine manifestations in combination with central and peripheral nervous system abnormalities. Reported signs and symptoms include postnatal growth retardation, moderate intellectual disability, hypogonadotropic hypogonadism, insulin-dependent diabetes mellitus, central hypothyroidism, demyelinating sensorimotor polyneuropathy, and cerebellar and pyramidal signs. Progressive hearing loss and a hypoplastic pituitary gland have also been described. Brain imaging shows moderate white matter abnormalities. |
Is a |
True |
Hypogonadotropic hypogonadism |
Inferred relationship |
Some |
|