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723405001: Microlissencephaly micromelia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3424449010 Microlissencephaly micromelia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3424450010 Microlissencephaly micromelia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3424451014 Basel Vanagaite Sirota syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microlissencephaly micromelia syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Microlissencephaly micromelia syndrome Is a Micromelia true Inferred relationship Existential restriction modifier
Microlissencephaly micromelia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Microlissencephaly micromelia syndrome Is a Lissencephaly true Inferred relationship Existential restriction modifier
Microlissencephaly micromelia syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Microlissencephaly micromelia syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 4
Microlissencephaly micromelia syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 4
Microlissencephaly micromelia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Microlissencephaly micromelia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Microlissencephaly micromelia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Microlissencephaly micromelia syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 6
Microlissencephaly micromelia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 7
Microlissencephaly micromelia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Microlissencephaly micromelia syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 7
Microlissencephaly micromelia syndrome Finding site Entire limb false Inferred relationship Existential restriction modifier 7
Microlissencephaly micromelia syndrome Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 5
Microlissencephaly micromelia syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier 3
Microlissencephaly micromelia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Microlissencephaly micromelia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microlissencephaly micromelia syndrome Finding site Entire limb true Inferred relationship Existential restriction modifier 1
Microlissencephaly micromelia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Microlissencephaly micromelia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Microlissencephaly micromelia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Microlissencephaly micromelia syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Microlissencephaly micromelia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Microlissencephaly micromelia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microlissencephaly micromelia syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 1
Microlissencephaly micromelia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microlissencephaly micromelia 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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