Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Mixed gonadal dysgenesis |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Other gonadal dysgenesis phenotype NOS |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Gonadal dysgenesis NOS |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Ovarian dysgenesis |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Testicular regression syndrome |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Congenital anomaly of ovary |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Pure gonadal dysgenesis |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Congenital anomaly of testis (disorder) |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Congenital anomaly of endocrine gonad (disorder) |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Congenital absence of gonads |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Congenital hypoplasia of gonad |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Accessory gonad |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
A rare syndrome described and characterized by prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome is characterised by sex reversal in males with a 46, XX (SRY-negative) karyotype, palmoplantar hyperkeratosis and a predisposition to squamous cell carcinoma. To date, five cases (four of whom were brothers) have been described. The aetiology is unknown. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
SERKAL (SEx Reversion, Kidneys, Adrenal and Lung dysgenesis) syndrome is characterized by female to male sex reversal and developmental anomalies of the kidneys, adrenal glands and lungs. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Splenogonadal fusion |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Male pseudohermaphroditism |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Störung der Geschlechtsentwicklung 46,XX, ovotestikuläre |
Is a |
False |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
Micro syndrome is an autosomal recessive disorder characterized by ocular and neurodevelopmental defects and by micro genitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|
46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome is a rare, genetic, developmental defect during embryogenesis disorder characterized by partial (unilateral testis, persistence of Müllerian duct structures) or complete (streak gonads only) gonadal dysgenesis, usually manifesting with primary amenorrhea in individuals with female phenotype but 46,XY karyotype, and sensorimotor dysmyelinating minifascicular polyneuropathy, which presents with numbness, weakness, exercise-induced muscle cramps, sensory disturbances and reduced/absent deep tendon reflexes. Germ cell tumors (seminoma, dysgerminoma, gonadoblastoma) may develop from the gonadal tissue. |
Is a |
True |
Gonadal dysgenesis |
Inferred relationship |
Some |
|