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1230021007: Frontorhiny (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5066437013 Frontorhiny (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066438015 ALX3-related frontonasal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066439011 Frontorhiny en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066440013 ALX homeobox 3-related frontonasal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066441012 Isolated median cleft face syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066442017 Frontonasal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400112011 A rare frontonasal dysplasia characterized by hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400113018 A rare frontonasal dysplasia characterised by hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066437013 Frontorhiny (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066438015 ALX3-related frontonasal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066439011 Frontorhiny en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066440013 ALX homeobox 3-related frontonasal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5066441012 Isolated median cleft face syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066442017 Frontonasal dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5066443010 A distinct syndromic type of frontonasal malformation with characteristics of hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400112011 A rare frontonasal dysplasia characterized by hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400113018 A rare frontonasal dysplasia characterised by hypertelorism, wide nasal bridge, broad columella, widened philtrum, widely separated narrow nares, poor development of nasal tip, midline notch of the upper alveolus, columella base swellings and a low hairline. Additional features reported in some include upper eyelid ptosis and midline dermoid cysts of craniofacial structures and philtral pits or rugose folding behind the ears. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3453031001000117 Frontorhinie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453031001000117 Frontorhinie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontorhiny (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Frontorhiny (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Frontorhiny (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Frontorhiny (disorder) Is a Frontonasal dysplasia sequence true Inferred relationship Existential restriction modifier (core metadata concept)
Frontorhiny (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Frontorhiny (disorder) Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Frontorhiny (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Frontorhiny (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Frontorhiny (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Frontorhiny (disorder) Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Frontorhiny (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Frontorhiny (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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