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717977003: Lissencephaly syndrome Norman Roberts type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3310760010 Lissencephaly syndrome Norman Roberts type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3310761014 Lissencephaly syndrome Norman Roberts type en Synonym Active Only initial character case insensitive SNOMED CT core module
3310762019 Microlissencephaly type A en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly syndrome Norman Roberts type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Is a Type 1 lissencephaly true Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Is a Congenital abnormality of skull and face bones true Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Lissencephaly syndrome Norman Roberts type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Lissencephaly syndrome Norman Roberts type Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Lissencephaly syndrome Norman Roberts type Finding site Bone structure of head false Inferred relationship Existential restriction modifier 5
Lissencephaly syndrome Norman Roberts type Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 3
Lissencephaly syndrome Norman Roberts type Finding site Brain structure false Inferred relationship Existential restriction modifier 3
Lissencephaly syndrome Norman Roberts type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Lissencephaly syndrome Norman Roberts type Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Lissencephaly syndrome Norman Roberts type Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 4
Lissencephaly syndrome Norman Roberts type Finding site Brain structure true Inferred relationship Existential restriction modifier 2
Lissencephaly syndrome Norman Roberts type Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Lissencephaly syndrome Norman Roberts type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Lissencephaly syndrome Norman Roberts type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Lissencephaly syndrome Norman Roberts type Finding site Bone structure of head true Inferred relationship Existential restriction modifier 1
Lissencephaly syndrome Norman Roberts type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Lissencephaly syndrome Norman Roberts type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Lissencephaly syndrome Norman Roberts type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Lissencephaly syndrome Norman Roberts type 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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