Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dysplastic ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital ovarian dysplasia |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Embryonic cyst of ovary (disorder) |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital cyst of canal of Nuck |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Female pseudohermaphroditism |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ovarian dysgenesis |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vesicular appendix of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ectopic ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital malposition of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hypoplasia of ovary (disorder) |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Accessory ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tubule of epoophoron |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Duct of epoophoron |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Paroophoron |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hypertrophy of ovary (disorder) |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of vas deferens |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of prostate |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of ovary |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atresia of ejaculatory duct |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital aplasia of round ligament |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital fusion of sacroiliac joint |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare genetic syndrome with limb reduction defects characterized by skeletal malformations comprising absent or hypoplastic pelvic bones (including sacral agenesis or hypoplasia), intercalary limb deficiencies (phocomelia potentially combined with polydactyly, oligodactyly or ectrodactyly), and skull defects (frequently a defect of the occipital bone with or without meningocele). Additional features may include thoracic dystrophy, dysmorphic facial features (dysplastic and large ears, and a high and narrow palate), and genital malformations (Mullerian aplasia, agenesis of the uterus and vagina, micropenis with cryptorchidism). Growth and mental development are not affected. |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of pelvis and lower limb |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ischiopagus |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dipygus |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital wide symphysis pubis (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital lumbosacral fusion |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Embryonic cyst of epoophoron |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hydrocele of canal of Nuck |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of seminal vesicle (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare syndromic central nervous system malformation characterised by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11. |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoplasia of sacrum |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sacral agenesis |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Holoprosencephaly with caudal dysgenesis syndrome |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital sacrococcygeal anomaly |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Caudal regression syndrome |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital sacral meningocele |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Sacral dysgenesis |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare, genetic, developmental defect during embryogenesis disorder characterised by varying degrees of caudal dysgenesis, ranging from a single umbilical artery or imperforate anus to full sirenomelia, in several members of the same family. Phenotype includes lumbosacral agenesis, anal atresia or ectopia, genitourinary abnormalities, components of VATER or VACTERL association, and facial dysmorphism (flat facies, abnormal ears, bilateral epicanthic folds, depressed nasal bridge, micrognathia). Additional features reported include cardiovascular (e.g. endocardial cushion defect, hypoplasia of pulmonary artery) and skeletal (kyphosis, hemipelvis) anomalies. |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital deformity of lumbosacral joint |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital agenesis of vagina |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hyperlordosis of lumbosacral spine |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|