Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Congenital anomaly of the pelvis |
Is a |
Sygdom i bækkenet |
false |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Is a |
Congenital anomaly of trunk |
false |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Finding site |
This structure, also termed the pelvic region, includes the wall, cavity and content of both the true and false pelvis; it consequently incorporates the entire bony pelvis; and inferiorly it is bounded and includes the pelvic diaphragm. The structure incorporates the complete pelvic wall; sacrococcygeal region (including the overlying skin and subcutaneous tissue); the contents of the false pelvic cavity; but in contrast to the 'pelvic segment of trunk' excludes the perineum, external genitalia. |
true |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Occurrence |
Congenital |
false |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Associated morphology |
kongenit anomali |
false |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Is a |
Congenital abnormality of lower limb and pelvic girdle |
false |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Is a |
Congenital anomaly of lower trunk |
true |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Finding site |
This structure, also termed the pelvic region, includes the wall, cavity and content of both the true and false pelvis; it consequently incorporates the entire bony pelvis; and inferiorly it is bounded and includes the pelvic diaphragm. The structure incorporates the complete pelvic wall; sacrococcygeal region (including the overlying skin and subcutaneous tissue); the contents of the false pelvic cavity; but in contrast to the 'pelvic segment of trunk' excludes the perineum, external genitalia. |
false |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Associated morphology |
kongenit anomali |
false |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Is a |
Disorder of pelvis |
true |
Inferred relationship |
Some |
|
|
Congenital anomaly of the pelvis |
Occurrence |
Congenital |
false |
Inferred relationship |
Some |
2 |
|
Congenital anomaly of the pelvis |
Associated morphology |
dysgenese |
false |
Inferred relationship |
Some |
2 |
|
Congenital anomaly of the pelvis |
Finding site |
This structure, also termed the pelvic region, includes the wall, cavity and content of both the true and false pelvis; it consequently incorporates the entire bony pelvis; and inferiorly it is bounded and includes the pelvic diaphragm. The structure incorporates the complete pelvic wall; sacrococcygeal region (including the overlying skin and subcutaneous tissue); the contents of the false pelvic cavity; but in contrast to the 'pelvic segment of trunk' excludes the perineum, external genitalia. |
false |
Inferred relationship |
Some |
2 |
|
Congenital anomaly of the pelvis |
Occurrence |
Congenital |
true |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Associated morphology |
Morphologically abnormal structure |
true |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Pathological process (attribute) |
Pathological developmental process |
true |
Inferred relationship |
Some |
1 |
|
Congenital anomaly of the pelvis |
Is a |
Congenital anomaly of abdomen |
false |
Inferred relationship |
Some |
|
|
Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dysplastic ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital ovarian dysplasia |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Embryonic cyst of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital cyst of canal of Nuck |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Female pseudohermaphroditism |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Ovarian dysgenesis |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Vesicular appendix of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Ectopic ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital malposition of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital hypoplasia of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Accessory ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Tubule of epoophoron |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Duct of epoophoron |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Paroophoron |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital hypertrophy of ovary |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital anomaly of vas deferens |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital anomaly of prostate |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital anomaly of ovary |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital atresia of ejaculatory duct |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital aplasia of round ligament |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital fusion of sacroiliac joint (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
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 |
Some |
|
Congenital absence of pelvis and lower limb |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Ischiopagus |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Dipygus |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital wide symphysis pubis (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital lumbosacral fusion |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Embryonic cyst of epoophoron |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital hydrocele of canal of Nuck (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital absence of seminal vesicle (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
A rare syndromic central nervous system malformation characterized 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 |
Some |
|
Hypoplasia of sacrum (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Sacral agenesis |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
A central nervous system malformation syndrome with characteristics of holoprosencephaly with microcephaly, abnormal eye morphology (hypotelorism, cyclopia, exophthalmos), nasal anomalies (single nostril or absent nose), and cleft lip/palate, combined with signs of caudal regression (sacral agenesis, sirenomelia with absent external genitalia). |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital sacrococcygeal anomaly |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Caudal regression syndrome |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital sacral meningocele |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Sacral dysgenesis |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
A rare, genetic, developmental defect during embryogenesis disorder characterized 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 |
Some |
|
Congenital deformity of lumbosacral joint (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital agenesis of vagina |
Is a |
False |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|
Congenital hyperlordosis of lumbosacral spine (disorder) |
Is a |
True |
Congenital anomaly of the pelvis |
Inferred relationship |
Some |
|