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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
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
13820591000172113 frontorhinie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
13820601000172115 frontonasale dysplasie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
13820611000172117 syndroom van geïsoleerde mediane aangezichtsspleet nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
13820621000172110 ALX-3-gerelateerde frontonasale dysplasie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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