Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Primary ovarian failure |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Primary testicular failure (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
X-linked intellectual disability Van Esch type (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
X-linked intellectual disability Cilliers type (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus with obesity and hypogonadism syndrome |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypogonadism with mitral valve prolapse and intellectual disability syndrome |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare syndromic endocrine disease characterized by the association of hypergonadotropic hypogonadism and cataracts with onset during adolescence. |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder) |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism. |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Woodhouse Sakati syndrome |
Is a |
True |
Primary hypogonadism (disorder) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|