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1172632008: SIX homeobox 2-related frontonasal dysplasia (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4634887019 SIX homeobox 2-related frontonasal dysplasia (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4634888012 SIX2-related frontonasal dysplasia en Synonym Active Case sensitive SNOMED CT core
4634889016 SIX homeobox 2-related frontonasal dysplasia en Synonym Active Case sensitive SNOMED CT core
4634890013 A rare frontonasal dysplasia with characteristics of a craniofacial phenotype comprising frontal bossing with high anterior hairline, ptosis, hypertelorism, epicanthus inversus, flat nasal bridge and broad nasal tip. Large anterior fontanel, sagittal synostosis, and cranial base anomalies have also been described. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
SIX2-related frontonasal dysplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
SIX2-related frontonasal dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
SIX2-related frontonasal dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
SIX2-related frontonasal dysplasia Is a Frontonasal dysplasia sequence true Inferred relationship Some
SIX2-related frontonasal dysplasia Occurrence Congenital true Inferred relationship Some 1
SIX2-related frontonasal dysplasia Finding site Bone structure of cranium true Inferred relationship Some 1
SIX2-related frontonasal dysplasia Associated morphology Dysplasia true Inferred relationship Some 1
SIX2-related frontonasal dysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
SIX2-related frontonasal dysplasia Occurrence Congenital true Inferred relationship Some 2
SIX2-related frontonasal dysplasia Finding site Face structure true Inferred relationship Some 2
SIX2-related frontonasal dysplasia Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
SIX2-related frontonasal dysplasia 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

Strength reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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