Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Deep full thickness burn of the genitalia, with loss of body part |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
1 |
Superficial foreign body of vagina without major open wound AND without infection |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
2 |
Deep full thickness burn of the genitalia, with loss of body part |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
1 |
Traumatic injury of external genitalia (disorder) |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
1 |
Traumatic injury of external genitalia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Superficial foreign body of vulva without major open wound AND without infection |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Superficial injury of vulva without infection |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Traumatic blister of vulva, infected |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
4 |
Nonvenomous insect bite of vulva with infection |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
2 |
Crush injury of labia |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Traumatic blister of vulva |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
4 |
Crush injury, vulva |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Ambiguous genitalia |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Ambiguous genitalia |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Duplication of external genitalia |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
Duplication of external genitalia |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Traumatic amputation of external genital organs |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
2 |
Injury to external genitalia due to birth trauma (disorder) |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
2 |
A rare disorder of sex development characterized by primary amenorrhea and ambiguous external genitalia (enlarged clitoris with marked fusion of the labioscrotal folds) in association with skeletal anomalies (such as hypoplasia of the mandibular condyles and the maxilla, and ulnar dislocation of the radial heads), in the presence of a 46,XX karyotype and regular ovaries, fallopian tubes, and uterus. There have been no further descriptions in the literature since 1972. |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
3 |
A rare multiple congenital anomalies syndrome characterised by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modelling of tubular bones, and reduced cutis laxa may become apparent later on. |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
7 |
Complex burn of genitalia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomalies syndrome characterised by variable skeletal abnormalities (including craniostenosis, pectus carinatum, short sternum, joint hyperextensibility, and abnormal vertebrae), cutis laxa with excessive skin folds around the cheek, chin and neck, ambiguous genitalia with a micropenis and perineal hypospadia, an umbilical hernia, intellectual disability, premature aged appearance, and cardiac enlargement involving either the ventricles or atria. Facial dysmorphism is variable and can include multiple hair whorls, ptosis, high and broad nasal root, low set ears and small chin. Enamel hypocalcification, abnormal modelling of tubular bones, and reduced cutis laxa may become apparent later on. |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
A rare disorder of sex development characterized by primary amenorrhea and ambiguous external genitalia (enlarged clitoris with marked fusion of the labioscrotal folds) in association with skeletal anomalies (such as hypoplasia of the mandibular condyles and the maxilla, and ulnar dislocation of the radial heads), in the presence of a 46,XX karyotype and regular ovaries, fallopian tubes, and uterus. There have been no further descriptions in the literature since 1972. |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Female pseudohermaphroditism |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Reifenstein syndrome |
Finding site |
False |
External genitalia structure |
Inferred relationship |
Some |
2 |
Male pseudohermaphroditism |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Vulval structure |
Is a |
True |
External genitalia structure |
Inferred relationship |
Some |
|
Pseudovaginal perineoscrotal hypospadias |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
A difference of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens. |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Normal external genitalia |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Injury to external genitalia due to birth trauma (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Traumatic amputation of external genital organs |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Genital edema |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Hemorrhage of genital region |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Structure of skin and/or mucosa of external genitalia (body structure) |
Is a |
True |
External genitalia structure |
Inferred relationship |
Some |
|
Mild androgen insensitivity syndrome |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Multiple injuries of external genitalia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Macrogenitosomia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Male pseudohermaphroditism due to congenital adrenal hyperplasia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Female pseudohermaphroditism due to congenital adrenal hyperplasia |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Male macrogenitosomia praecox |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
3 |
Macrogenitosomia praecox due to disorder of pineal gland (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Robinow syndrome (RS) is a rare genetic syndrome characterized by limb shortening and abnormalities of the head, face and external genitalia. |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
3 |
Autosomal recessive Robinow syndrome |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
7 |
The more common type of Robinow syndrome characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia. |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
7 |
Finding of quantity of smegma |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Finding of smegma |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Lack of smegma |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Smegma offensive |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Finding of odor of smegma |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Excessive smegma |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
2 |
Bite wound of external genitalia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Abrasion of genitalia |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Plain X-ray of external genitalia |
Procedure site - Direct (attribute) |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |
Congenital hypoplasia of external genitalia (disorder) |
Finding site |
True |
External genitalia structure |
Inferred relationship |
Some |
1 |