| 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 |
|