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1230021007: Frontorhiny (disorder)


Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5066437013 Frontorhiny (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5066438015 ALX3-related frontonasal dysplasia en Synonym Active Case sensitive SNOMED CT core
5066439011 Frontorhiny en Synonym Active Case insensitive SNOMED CT core
5066440013 ALX homeobox 3-related frontonasal dysplasia en Synonym Active Case sensitive SNOMED CT core
5066441012 Isolated median cleft face syndrome en Synonym Active Case insensitive SNOMED CT core
5066442017 Frontonasal dysplasia type 1 en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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