| 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 | 
  |