72914001: Palatal structure (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure\Head part\Structure of subregion of head\Palatal 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

121108013 Palate en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

502287011 Palatal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

813244012 Palatal structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Palatal structure	Is a	Lip and/or palatal structures	false	Inferred relationship	Some
Palatal structure	partie de	Entire mouth region	false	Additional relationship	Some
Palatal structure	Is a	Head part	false	Inferred relationship	Some
Palatal structure	Is a	Oral cavity structure	false	Inferred relationship	Some
Palatal structure	Is a	Structure of internal part of mouth	false	Inferred relationship	Some
Palatal structure	Is a	Structure of subregion of head	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome is a rare, genetic, orofacial clefting malformation syndrome characterized by severe frontonasal dysplasia with complete cleft palate, facial cleft, extreme microphthalmia and hypertelorism, frequently associated with eyelid colobomata, sparse or absent eyelashes/eyebrows, wide nasal bridge with hypoplastic alae nasi, low-set, posteriorly rotated ears and caudal appendage in the sacral region.	Finding site	True	Palatal structure	Inferred relationship	Some	1
A rare, syndromic, developmental defect of the eye malformation characterized by unilateral or bilateral, single or multiple, filiforme bands of elastic tissue which connect the eyelid margins at the gray line, associated with cleft lip and palate. Eye examination is otherwise normal.	Finding site	True	Palatal structure	Inferred relationship	Some	1
Structure of left half of palate (body structure)	Is a	True	Palatal structure	Inferred relationship	Some
Structure of right half of palate (body structure)	Is a	True	Palatal structure	Inferred relationship	Some
Incomplete cleft palate (disorder)	Finding site	True	Palatal structure	Inferred relationship	Some	1
Repair of defect of palate with skin graft	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
Structure of superior aspect of palate (body structure)	Is a	True	Palatal structure	Inferred relationship	Some
Structure of inferior aspect of palate (body structure)	Is a	True	Palatal structure	Inferred relationship	Some
Palatal exercises	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	1
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	Palatal structure	Inferred relationship	Some	2
Palatopharyngoplasty	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
Gordon syndrome, also known as distal arthrogryposis type 3, is an extremely rare multiple congenital malformation syndrome characterized by congenital contractures of hand and feet with variable degrees of severity of camptodactyly, clubfoot and, less frequently, cleft palate. Intelligence is normal but in some cases, additional abnormalities, such as short stature, kyphoscoliosis, ptosis, micrognathia, and cryptorchidism may also be present. Gordon syndrome, Marden-Walker syndrome and arthrogryposis with oculomotor limitation and electroretinal anomalies clinically and genetically overlap, and could represent variable expressions of the same condition.	Finding site	True	Palatal structure	Inferred relationship	Some	1
Ecchymosis of palate	Finding site	True	Palatal structure	Inferred relationship	Some	1
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome is a rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, axial hypotonia, palate abnormalities (including cleft palate and/or high and narrow palate), dysmorphic facial features (including prominent forehead, hypertelorism, downslanting palpebral fissures, wide nasal bridge, thin lips and widely spaced teeth), and short stature. Additional manifestations may include digital anomalies (such as brachydactyly, clinodactyly, and hypoplastic toenails), a single palmar crease, lower limb hypertonia, joint hypermobility, as well as ocular and urogenital anomalies.	Finding site	True	Palatal structure	Inferred relationship	Some	2
Structure of muscle of palate	Is a	True	Palatal structure	Inferred relationship	Some
Primary Kaposi sarcoma of palate (disorder)	Finding site	True	Palatal structure	Inferred relationship	Some	1
Primary Kaposi sarcoma of palate (disorder)	Finding site	False	Palatal structure	Inferred relationship	Some	2
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	Palatal structure	Inferred relationship	Some	2
Mass of palate	Finding site	True	Palatal structure	Inferred relationship	Some	1
Laser uvulectomy and palatal scarring	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
Primary salivary gland type carcinoma of palate (disorder)	Finding site	True	Palatal 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	Palatal structure	Inferred relationship	Some	5
Repair of anterior palatal fistula with gingival flap	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	3
Repair of cleft palate using pharyngeal flap (procedure)	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
Pharyngoplasty for cleft palate	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
Metastatic carcinoma to palate (disorder)	Finding site	True	Palatal structure	Inferred relationship	Some	1
Primary palate carcinoma (disorder)	Finding site	True	Palatal structure	Inferred relationship	Some	1
Fitting of palatal lift prosthesis	Procedure site - Indirect (attribute)	True	Palatal structure	Inferred relationship	Some	1
Insertion of palatal lift prosthesis	Procedure site - Indirect (attribute)	True	Palatal structure	Inferred relationship	Some	1
Grafting of palate for cleft palate repair (procedure)	Procedure site - Direct (attribute)	True	Palatal structure	Inferred relationship	Some	2
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of congenital heart defect (including atrial or ventricular septal defects and aortic coarctation), cleft palate, and variable degree of developmental delay and intellectual disability. Most patients reported to also have autism spectrum disorder. Overlapping facial features were reported in some patients including broad forehead with high anterior hairline, finely arched eyebrows, short philtrum, thin or tented upper lip. Other clinical features may involve mild distal skeletal abnormalities, hypotonia, hearing loss, feeding problems and skin abnormalities.	Finding site	True	Palatal structure	Inferred relationship	Some	1
High palate (finding)	Finding site	True	Palatal structure	Inferred relationship	Some	1
Narrow palate (finding)	Finding site	True	Palatal structure	Inferred relationship	Some	1

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Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
121108013	Palate	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502287011	Palatal structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
813244012	Palatal structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core