| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Testicular tumor of adrenogenital syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Testicular tumor of adrenogenital syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Severe steroid 21-hydroxylase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Transitory amino acid metabolic disorder | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Iodotyrosine deiodination defect | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal dominant variant form of albumin | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Neonatal iminoglycinuria | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Maturity onset diabetes mellitus in young | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial adrenocortical hypoplasia | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Placental sulfatase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Cholesterol monooxygenase (side-chain cleaving) deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Corticosterone 18-monooxygenase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 17 alpha-Hydroxyprogesterone aldolase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Testosterone 17-beta-dehydrogenase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Transient neonatal hyperglycinemia | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Steroid 21-monooxygenase deficiency, simple virilizing type | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 3 beta-Hydroxysteroid dehydrogenase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Moderate steroid 21-hydroxylase deficiency | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hereditary nephrogenic diabetes insipidus | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Adrenoleukodystrophy | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Autosomal dominant excess of transthyretin | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Benign neonatal hyperaminoaciduria | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hereditary adrenal unresponsiveness to corticotropin | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hereditary vitamin D dependency syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Transient neonatal hypertyrosinemia | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Neonatal hyperhistidinemia | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Opitz-Frias syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Pseudohypoaldosteronism, type 1, dominant form | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Pseudohypoaldosteronism, type 1, recessive form | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| WNT4 Müllerian aplasia and ovarian dysfunction | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Sensorineural deafness and male infertility | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypogonadism with prune belly syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Prominent glabella with microcephaly and hypogenitalism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Short stature with craniofacial anomalies and genital hypoplasia syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability and short stature with hand contracture and genital anomaly syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial hypospadias of penis | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hereditary breast and ovarian cancer syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Deafness and hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability Van Esch type | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability Cilliers type | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Syndromic X-linked intellectual disability type 7 | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Primary hypergonadotropic hypogonadism and partial alopecia syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability with precocious puberty and obesity syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Chondrodysplasia with disorder of sex development syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hydrocephalus with obesity and hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypergonadotropic hypogonadism with cataract syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, balding, patella luxation, acromicria syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypogonadism with anosmia | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital cataract with deafness and hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome | Is a | False | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Sex reversion, kidney, adrenal and lung dysgenesis syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Frontonasal dysplasia with alopecia and genital anomaly syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 46,XY partial gonadal dysgenesis | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial male-limited precocious puberty | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Splenogonadal fusion, limb defect, micrognathia syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Spastic paraplegia with precocious puberty syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Dysmorphism, short stature, deafness, disorder of sex development syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| XY type gonadal dysgenesis with associated anomalies syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 46,XX disorder of sex development with skeletal anomalies syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Intellectual disability, myopathy, short stature, endocrine defect syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Female infertility due to zona pellucida defect | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Alopecia, progressive neurological defect, endocrinopathy syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hereditary site-specific ovarian cancer syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| X-linked central congenital hypothyroidism with late-onset testicular enlargement | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| RAB18, member RAS oncogene family deficiency | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Genitopalatocardiac syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Leydig cell agenesis | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Familial adrenal hypoplasia with absent pituitary luteinizing hormone | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| 46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Hyperandrogenism due to cortisone reductase deficiency | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Obesity due to leptin receptor gene deficiency | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Partial androgen insensitivity syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Diabetes, hypogonadism, deafness, intellectual disability syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Progressive cerebellar ataxia with hypogonadism | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Ovarioleukodystrophy | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  | 
| Female infertility due to oocyte meiotic arrest | Is a | True | Reproductive system hereditary disorder | Inferred relationship | Existential restriction modifier |  |