Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Penile hypospadias (disorder) |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Penoscrotal hypospadias (disorder) |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Perineal hypospadias (disorder) |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
glandulær hypospadi |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Opitz-Frias syndrome |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Female hypospadias (disorder) |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
[X]Other specified hypospadias |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Urethroplasy with skin graft for second stage hypospadias repair (procedure) |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Male subcoronal hypospadias |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Scrotal hypospadias |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Congenital prolapse of urinary meatus (disorder) |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
History of congenital hypospadias (situation) |
Associated finding |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
1 |
Family history of hypospadias (situation) |
Associated finding |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
1 |
A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and characterized by hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked nails. |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome is characterized by symmetric, nonopposable triphalangeal thumbs and radial hypoplasia. It has been described in eight patients (five females and three males) spanning generations of a family. The affected males also presented with hypospadias. The syndrome is inherited as an autosomal dominant trait. |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Hypospadias, hypertelorism, coloboma, deafness syndrome |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Repair of hypospadias urethroplasty using glanular flap |
Has focus |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Lower limb malformation-hypospadias syndrome is a rare developmental defect during embryogenesis characterized by severe, uni- or bilateral lower limb malformations (including tibial hypoplasia, split and rocker bottom-shaped feet, and oligosyndactyly), normal upper limbs and hypospadias. Additional dysmorphic features (e.g. short neck and low-set, large ears), atrial septal defect, ureteropelvic junction stenosis and slight septation of the spleen, have also been reported. There have been no further descriptions in the literature since 1977. |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Spondylocostal dysostosis, hypospadias, intellectual disability syndrome |
Is a |
False |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Posterior hypospadias is a rare, non-syndromic, urogenital tract malformation with characteristics of an ectopic urethral meatus opening located in the posterior penis, the penoscrotal junction, the scrotum or the perineum, which often appears stenotic. The scrotum might appear bifid in severe cases and micropenis is not commonly associated. Urinary tract malformations, such as ureteropelvic junction obstruction, vesicoureteric reflux, pelvic or horseshoe kidney, crossed renal ectopia, renal agenesis, may be observed. |
Is a |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
|
Male hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Revision of hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Simple repair of hypospadias complications |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Reconstruction by urethra-meatal advancement |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Reconstruction by urethra-ventralising operation |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Non-prepucial skin flap reconstruction of urethra |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Duckett hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Asopa hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Harris hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |
Denis-Browne hypospadias repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Repair of hypospadias using onlay patch (procedure) |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Repair of hypospadias using double faced onlay patch |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Tubularized incised plate urethroplasty (procedure) |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
2 |
Hypospadias and chordee repair |
Has focus |
True |
Hypospadias (disorder) |
Inferred relationship |
Some |
3 |