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87528003: Structure of urethral meatus (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
145114019 Urethral meatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
507624016 Structure of urethral meatus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
830020013 Structure of urethral meatus (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4455951000005110 struktur af meatus urethrae da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of urethral meatus Is a External body orifice false Inferred relationship Some
Structure of urethral meatus Is a uretral åbning false Inferred relationship Some
Structure of urethral meatus del af Entire urethra false Additional relationship Some
Structure of urethral meatus Is a Urethra part true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Ulcer of urethral meatus Finding site False Structure of urethral meatus Inferred relationship Some 1
Urethral caruncle Finding site True Structure of urethral meatus Inferred relationship Some 1
Swab from urethral meatus (specimen) Specimen source topography (attribute) True Structure of urethral meatus Inferred relationship Some 1
Congenital stricture of urinary meatus Finding site False Structure of urethral meatus Inferred relationship Some 3
Atresia of urinary meatus Finding site False Structure of urethral meatus Inferred relationship Some 2
Congenital urinary meatus obstruction (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 3
Male subcoronal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 1
Penoscrotal hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
glandulær hypospadi Finding site False Structure of urethral meatus Inferred relationship Some 3
Perineal hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Female hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 3
Male subcoronal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 2
Opitz-Frias syndrome Finding site False Structure of urethral meatus Inferred relationship Some 4
Glanular hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 5
Coronal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 5
Penile hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 3
Distal penile hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 2
Proximal penile hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Penile shaft hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Penile mid-shaft hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Scrotal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 2
Urethral parameatal cyst (disorder) Finding site False Structure of urethral meatus Inferred relationship Some
Congenital prolapse of urinary meatus (disorder) Finding site True Structure of urethral meatus Inferred relationship Some 1
Penile hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
Perineal hypospadias (disorder) Finding site True Structure of urethral meatus Inferred relationship Some 1
glandulær hypospadi Finding site False Structure of urethral meatus Inferred relationship Some 2
Hypospadias (disorder) Finding site True Structure of urethral meatus 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. Finding site False Structure of urethral meatus Inferred relationship Some 2
Familial hypospadias of penis (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 3
Familial hypospadias of penis (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 2
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. Finding site False Structure of urethral meatus Inferred relationship Some 8
Hypospadias, hypertelorism, coloboma, deafness syndrome Finding site False Structure of urethral meatus Inferred relationship Some 6
Stenosis of urinary meatus Finding site True Structure of urethral meatus Inferred relationship Some 2
Spina bifida-hypospadias syndrome is a rare developmental defect during embryogenesis disorder characterized by the specific association of glandular hypospadias and lumbo-sacral spina bifida. Affected individuals may or may not present additional congenital anomalies, such as hydrocephaly, microstomia, patent ductus arteriosus, cryptorchidism, intestinal malrotation, rocker-bottom feet, and hypertrichosis. Finding site False Structure of urethral meatus Inferred relationship Some 6
Urethral parameatal cyst (disorder) Finding site True Structure of urethral meatus Inferred relationship Some 1
Congenital parameatal cyst Finding site True Structure of urethral meatus Inferred relationship Some 1
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. Finding site True Structure of urethral meatus Inferred relationship Some 2
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. Finding site False Structure of urethral meatus Inferred relationship Some 1
Female hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 1
Coronal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 1
Glanular hypospadias Finding site False Structure of urethral meatus 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. Finding site True Structure of urethral meatus Inferred relationship Some 1
Coronal hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 2
Glanular hypospadias Finding site False Structure of urethral meatus Inferred relationship Some 2
Opitz-Frias syndrome Finding site False Structure of urethral meatus Inferred relationship Some 2
Penoscrotal hypospadias (disorder) Finding site False Structure of urethral meatus Inferred relationship Some 1
Hypospadias, hypertelorism, coloboma, deafness syndrome Finding site False Structure of urethral meatus Inferred relationship Some 3
Spina bifida-hypospadias syndrome is a rare developmental defect during embryogenesis disorder characterized by the specific association of glandular hypospadias and lumbo-sacral spina bifida. Affected individuals may or may not present additional congenital anomalies, such as hydrocephaly, microstomia, patent ductus arteriosus, cryptorchidism, intestinal malrotation, rocker-bottom feet, and hypertrichosis. Finding site False Structure of urethral meatus Inferred relationship Some 5
Spondylocostal dysostosis, hypospadias, intellectual disability syndrome Finding site False Structure of urethral meatus Inferred relationship Some 2
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. Finding site True Structure of urethral meatus Inferred relationship Some 4
Spondylocostal dysostosis, hypospadias, intellectual disability syndrome Finding site False Structure of urethral meatus Inferred relationship Some 3
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. Finding site True Structure of urethral meatus Inferred relationship Some 1
Urethromeatoplasty with mucosal advancement Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 2
First stage of two-stage epispadias repair Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 1
Second stage of two-stage epispadias repair Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 2
Epispadias (disorder) Finding site True Structure of urethral meatus Inferred relationship Some 1
Epispadias repair Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 1
Single stage epispadias repair Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 1
Revision of hypospadias repair Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 1
Simple repair of hypospadias complications Procedure site - Direct (attribute) True Structure of urethral meatus Inferred relationship Some 1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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