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1177166006: Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder)


Status: current, Primitive. Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4643796019 Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome en Synonym Active Case insensitive SNOMED CT core
4643797011 Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4643798018 A rare syndromic frontonasal dysplasia with characteristics of distinctive facial dysmorphic features including hypertelorism, almond-shaped palpebral fissures, nasal deformity with creased ridge, depressed or absent tip and asymmetry and partial absence of nasal bones and downturned corners of the mouth. Additional reported manifestations are limb anomalies (e. g. Poland anomaly, transverse limb agenesis and anomalies of the hands and feet such as camptodactyly, oligodactyly, clinodactyly and syndactyly), frontonasal encephalocele, choanal atresia, congenital renal/cardiac malformations, and corpus callosum agenesis. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Is a Genetic disease true Inferred relationship Some
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Is a Frontonasal dysplasia sequence true Inferred relationship Some
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Occurrence Congenital true Inferred relationship Some 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Finding site Bone structure of cranium true Inferred relationship Some 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Occurrence Congenital true Inferred relationship Some 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Finding site Face structure true Inferred relationship Some 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome 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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