Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
RAB18, member RAS oncogene family deficiency (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
syndrome d'hypogonadisme hypogonadotrope-microcéphalie sévère-surdité neurosensorielle-dysmorphie |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Genitopalatocardiac syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Leydig cell agenesis (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hyperandrogenism due to cortisone reductase deficiency |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Obesity due to leptin receptor gene deficiency |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
syndrome d'insensibilité partielle aux androgènes |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Woodhouse Sakati syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Progressive cerebellar ataxia with hypogonadism |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Ovarioleukodystrophy |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Female infertility due to oocyte meiotic arrest |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Kallman syndrome with heart disease (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
4H leukodystrophy (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
46,XY disorder of sex development due to isolated 17,20-lyase deficiency (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Severe steroid 21-hydroxylase deficiency |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Transitory amino acid metabolic disorder |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Iodotyrosine deiodination defect |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant variant form of albumin |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Neonatal iminoglycinuria |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Maturity onset diabetes mellitus in young |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Testicular tumor of adrenogenital syndrome (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Familial adrenocortical hypoplasia |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Placental sulphatase deficiency |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Cholesterol monooxygenase (side-chain cleaving) deficiency |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Corticosterone 18-monooxygenase deficiency (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
17 alpha-Hydroxyprogesterone aldolase deficiency (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Testosterone 17-beta-dehydrogenase deficiency (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Transient neonatal hyperglycinaemia |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Steroid 21-monooxygenase deficiency, simple virilising type |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
3 beta-Hydroxysteroid dehydrogenase deficiency (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Moderate steroid 21-hydroxylase deficiency (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary nephrogenic diabetes insipidus |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Adrenoleukodystrophy |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant excess of transthyretin |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Benign neonatal hyperaminoaciduria |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary adrenal unresponsiveness to corticotropin |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary vitamin D dependency syndrome |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Transient neonatal hypertyrosinemia |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Neonatal hyperhistidinemia |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Opitz-Frias syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Pseudohypoaldosteronism, type 1, dominant form |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Pseudohypoaldosteronism, type 1, recessive form |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Testicular tumor of adrenogenital syndrome |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
WNT4 Mullerian aplasia and ovarian dysfunction |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Sensorineural deafness and male infertility |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hypogonadism with prune belly syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Prominent glabella with microcephaly and hypogenitalism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Familial hypospadias of penis (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
X-linked lissencephaly with abnormal genitalia syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary breast and ovarian cancer syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Deafness and hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
X-linked intellectual disability Van Esch type (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
X-linked intellectual disability Cilliers type (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Syndromic X-linked intellectual disability type 7 (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
X-linked intellectual disability with precocious puberty and obesity syndrome (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Chondrodysplasia with disorder of sex development syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hydrocephalus with obesity and hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hypergonadotropic hypogonadism with cataract syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, balding, patella luxation, acromicria syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
dysplasie olfactogénitale |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract with deafness and hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
False |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
46,XY partial gonadal dysgenesis (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Familial male-limited precocious puberty (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Splenogonadal fusion, limb defect, micrognathia syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Spastic paraplegia with precocious puberty syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Dysmorphism, short stature, deafness, disorder of sex development syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
XY type gonadal dysgenesis with associated anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
46,XX disorder of sex development with skeletal anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|
SCARF syndrome |
est un(e) (attribut) |
True |
Reproductive system hereditary disorder |
Inferred relationship |
Some |
|