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48477009: Lip structure (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
80770013 Lip en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495110012 Lip structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
786049011 Lip structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
881711000172117 lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
894771000172113 structure de la lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956691000172114 labium oris fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
979881000172115 lèvre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6997821000241112 structure d'une lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


105 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lip structure Is a Structure of oral region of face true Inferred relationship Some
Lip structure Is a Lip and/or palatal structures false Inferred relationship Some
Lip structure Is a Oral soft tissue structure true Inferred relationship Some
Lip structure partie de Entire oral region of face false Additional relationship Some
Lip structure Is a Structure of soft tissue of face (body structure) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Complete left cleft lip and complete cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Lip adhesion of left cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Lip adhesion of right cleft lip (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Repair of left cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Repair of right cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Plasma cell cheilitis Finding site True Lip structure Inferred relationship Some 1
Right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Left cleft lip Finding site False Lip structure Inferred relationship Some 1
Repair of right cleft lip with rotation advancement flap (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Incomplete right cleft lip Finding site False Lip structure Inferred relationship Some 1
Complete right cleft lip and complete cleft of right alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 1
Incomplete left cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Repair of left cleft lip with rotation advancement flap (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Complete right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Complete left cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Actinic cheilitis Finding site True Lip structure Inferred relationship Some 1
Complete left cleft lip and complete cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 1
Bilateral complete cleft lip and bilateral complete cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 1
Cleft lip and cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Lip incompetence due to horizontal overbite (finding) Finding site True Lip structure Inferred relationship Some 1
Acquired ectropion of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Primary syphilis of lip Finding site True Lip structure Inferred relationship Some 1
Pilotto syndrome Finding site True Lip structure Inferred relationship Some 2
Cleft hard and soft palate with right cleft lip and cleft of right alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft soft palate with left cleft lip and cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft of soft palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
A rare multiple congenital malformation syndrome, characterized by an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension etc.) and obstructive renal disease (ectopic ureteric insertion, obstruction, vesicoureteral reflux and hydronephrosis). Gastrointestinal tract involvement (malrotation, gastroesophageal reflux etc.) and cardiac involvement (coarctation of aorta, pulmonary artery stenosis, etc.) have also been reported. An overlap with Kabuki syndrome is debated. Finding site True Lip structure Inferred relationship Some 3
Bilateral incomplete cleft palate with cleft lip Finding site False Lip structure Inferred relationship Some 2
An exceedingly rare association characterized by cleft lip and progressive retinopathy. Finding site True Lip structure Inferred relationship Some 1
Cleft hard palate with right cleft lip and cleft of right alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by the association of auricular abnormalities (such as external ear abnormalities and postauricular pits) and cleft lip with or without cleft palate. Additional manifestations include myopia, nystagmus, and retinal pigment abnormalities. Finding site True Lip structure Inferred relationship Some 1
Cheilognathoschisis Finding site True Lip structure Inferred relationship Some 2
Cleft soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft soft palate with right cleft lip and cleft of right alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 2
Cleft hard and soft palate with left cleft lip and left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 4
Cleft hard palate with right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Hypertelorism-microtia-facial clefting syndrome, or HMC syndrome, is a very rare syndrome characterized by the combination of hypertelorism, cleft lip and palate and microtia. Finding site True Lip structure Inferred relationship Some 3
Cleft hard palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 1
Cleft hard palate with left cleft lip and cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 1
Granulomatous cheilitis Finding site True Lip structure Inferred relationship Some 1
Cleft soft palate with left cleft lip Finding site False Lip structure Inferred relationship Some 1
Exfoliative cheilitis Finding site True Lip structure Inferred relationship Some 1
Idiopathic exfoliative cheilitis (disorder) Finding site True Lip structure Inferred relationship Some 1
Cleft hard and soft palate with left cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Cleft palate with left cleft lip Finding site False Lip structure Inferred relationship Some 1
Cleft hard and soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 3
Microbrachycephaly-ptosis-cleft lip syndrome is characterized by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive. Finding site True Lip structure Inferred relationship Some 3
Cleft hard and soft palate with right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Overlapping neoplasm of oral cavity and lip and salivary gland Finding site True Lip structure Inferred relationship Some 2
Harlequin ichthyosis Finding site True Lip structure Inferred relationship Some 2
Holzgreve syndrome is an extremely rare, lethal, multiple congenital anomalies/dysmorphic syndrome characterized by renal agenesis with Potter sequence, cleft lip/palate, oral synechiae, cardiac defects, and skeletal abnormalities including postaxial polydactyly. Intestinal nonfixation and intrauterine growth restriction are also associated. There have been no further descriptions in the literature since 1988. Finding site True Lip structure Inferred relationship Some 1
Fetal cleft lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Melanotic macule of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Lentigo of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2
Pitting oedema of lip Finding site True Lip structure Inferred relationship Some 1
Contact cheilitis Finding site False Lip structure Inferred relationship Some 1
Angioedema of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Structure of fetal lip (body structure) Is a True Lip structure Inferred relationship Some
Superficial foreign body in lip Finding site True Lip structure Inferred relationship Some 1
Harlequin fetus Finding site True Lip structure Inferred relationship Some 2
Structure of skin and/or subcutaneous tissue of lip (body structure) Is a True Lip structure Inferred relationship Some
Superficial foreign body of lip with infection Finding site True Lip structure Inferred relationship Some 1
Dry lips Finding site True Lip structure Inferred relationship Some 2
Application of ointment to lip via topical route (procedure) Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Neoplasm of oral cavity and lip and salivary gland Finding site True Lip structure Inferred relationship Some 2
Malignant neoplasm of oral cavity and lip and salivary gland (disorder) Finding site True Lip structure Inferred relationship Some 2
Characterized by upper and lower incisors that have emerged forward making the teeth and lips protrude. Finding site True Lip structure Inferred relationship Some 3
Abrasion and/or friction burn of lip with infection (disorder) Finding site True Lip structure Inferred relationship Some 2
Mass of lip (finding) Finding site True Lip structure Inferred relationship Some 1
A rare genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability characterized by unilateral or bilateral cleft lip and palate and craniofacial dysmorphism (including frontal bossing, hypertelorism, broad flat nasal bridge, cupped ears/thickened helices, and micrognathia). Additional manifestations are variable congenital cardiac anomalies, pectus excavatum, abnormalities of the hands and feet, ocular abnormalities (myopia, cataract, staphyloma), and conductive or sensorineural hearing loss. Finding site True Lip structure Inferred relationship Some 1
Pedicle myocutaneous flap to lip Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Full thickness excision of lip, reconstruction with local flap Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 2
Reconstruction of lip using pedicle flap Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Local myocutaneous flap to lip (procedure) Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
A rare developmental defect during embryogenesis disorder characterized by spinal dysraphism, cleft lip and palate, limb reduction defects and anencephaly. There have been no further descriptions in the literature since 1994. Finding site True Lip structure Inferred relationship Some 1
Reconstruction of lip with tongue flap (procedure) Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 2
Reconstruction of lip using free myocutaneous flap with microvascular anastomosis (procedure) Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Metastatic carcinoma to lip Finding site True Lip structure Inferred relationship Some 1
Overlapping malignant neoplasm of oral cavity and lip and salivary gland (disorder) Finding site True Lip structure Inferred relationship Some 2
Primary carcinoma of lip Finding site True Lip structure Inferred relationship Some 1
Open wound of lip due to human bite Finding site True Lip structure Inferred relationship Some 1
Plain X-ray of lip (procedure) Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Cleft lip nasal deformity Finding site True Lip structure Inferred relationship Some 2
An isolated non syndromic fissure type embryopathy extending from the upper lip to the nasal base. The cleft is paramedian and located at the level of the philtrum. It presents as a cutaneous, muscular, and mucosal interruption from the lip to the nasal base, associated with nostril and nasal septum deformations. Clinical forms range from a simple notch in the upper lip to a complete cleft lip with an opening at the base of the nostril without reaching as far as the gum (alveolar ridge). This embryopathy appears between the 5th and 12th week of pregnancy due to a failure in the fusion of the frontal processes (fronto-nasal process, medial and lateral nasal processes, maxillary process). Finding site True Lip structure Inferred relationship Some 1
Lip discolouration Finding site True Lip structure Inferred relationship Some 1
Lip tremor (finding) Finding site True Lip structure Inferred relationship Some 1
Pursed appearance of lips Finding site True Lip structure Inferred relationship Some 1
Dribbling from mouth Finding site True Lip structure Inferred relationship Some 2
Nonvenomous insect bite of lip (disorder) Finding site True Lip structure Inferred relationship Some 1

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Reference Sets

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

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

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