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41194006: Bilobed structure (morphologic abnormality)

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
68717014 Bilobed structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
68720018 Bifid structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
777955015 Bilobed structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bilobed structure Is a Congenital septation false Inferred relationship Some
Bilobed structure Is a Morphologically abnormal structure true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Bilobed right lung Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid thumb Associated morphology False Bilobed structure Inferred relationship Some 1
Sternum bifidum Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid patella Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid tongue Associated morphology False Bilobed structure Inferred relationship Some 1
Congenital bilobed gallbladder Associated morphology True Bilobed structure Inferred relationship Some 1
Bifid digit Associated morphology False Bilobed structure Inferred relationship Some 1
Sternum bifidum Associated morphology True Bilobed structure Inferred relationship Some 1
Bifid thumb Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid tongue Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid digit Associated morphology False Bilobed structure Inferred relationship Some 1
Congenital bilobed gallbladder Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid patella Associated morphology False Bilobed structure Inferred relationship Some 1
Bilobed right lung Associated morphology True Bilobed structure Inferred relationship Some 1
Left lung isomerism is a congenital condition in which both lungs develop with the anatomical structure of a left lung. Normally, the left lung has two lobes (upper and lower), while the right lung has three lobes (upper, middle, and lower). In this condition, however, the abnormal right lung is also bilobed, resulting in bilateral bilobed lungs. Associated morphology True Bilobed structure Inferred relationship Some 1
Bifid thumb Associated morphology False Bilobed structure Inferred relationship Some 2
Congenital bilobed gallbladder Associated morphology False Bilobed structure Inferred relationship Some 2
Bifid kidney Associated morphology False Bilobed structure Inferred relationship Some 1
Bifid scrotum Associated morphology False Bilobed structure Inferred relationship Some 3
Bifid scrotum Associated morphology True Bilobed structure Inferred relationship Some 1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. Associated morphology False Bilobed structure Inferred relationship Some 4
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. Associated morphology False Bilobed structure Inferred relationship Some 5
BNAR syndrome is a very rare multiple congenital anomaly syndrome characterized by a bifid nose (with bulbous nasal tip but not associated with hypertelorism) with or without the presence of anal defects (i.e. anteriorly placed anus, rectal stenosis or atresia) and renal dysplasia and without intellectual disability. BNAR syndrome is phenotypically related to Fraser syndrome and oculotrichoanal syndrome. Associated morphology False Bilobed structure Inferred relationship Some 1
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by moderate to severe intellectual disability, congenital aphonia, hearing loss, optic atrophy, retinal dystrophy, broad thumbs and duplicated halluces. Facial dysmorphism (including thick eyebrows, ptosis, long, downslanting palpebral fissures, microstomia, low-set, posteriorly rotated ears) and genital abnormalities are also associated. Associated morphology True Bilobed structure Inferred relationship Some 1
Bilobate placenta Associated morphology True Bilobed structure Inferred relationship Some 1

This concept is not in any reference sets

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