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773628009: Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3724878013 Frontonasal dysplasia type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3724879017 ALX1-related frontonasal dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module
3724880019 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3724881015 ALX1 (aristaless-like homeobox 1) related frontonasal dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module
3724882010 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Cleft palate true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Microphthalmos true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier 4
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Finding site Palatal structure true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 4
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Finding site Entire eye true Inferred relationship Existential restriction modifier 3
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Developmental failure of fusion true Inferred relationship Existential restriction modifier 1
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 3
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Frontonasal dysplasia sequence true Inferred relationship Existential restriction modifier
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 4
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Associated morphology Developmental failure of fusion false Inferred relationship Existential restriction modifier 5
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 5
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Finding site Bone structure of head false Inferred relationship Existential restriction modifier 5
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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