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722283003: Agnathia, holoprosencephaly, situs inversus syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3331427010 Agnathia, holoprosencephaly, situs inversus syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3331429013 Agnathia, holoprosencephaly, situs inversus 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
Agnathia, holoprosencephaly, situs inversus syndrome Is a Holoprosencephaly sequence true Inferred relationship Existential restriction modifier
Agnathia, holoprosencephaly, situs inversus syndrome Is a Congenital micrognathism true Inferred relationship Existential restriction modifier
Agnathia, holoprosencephaly, situs inversus syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Agnathia, holoprosencephaly, situs inversus syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Agnathia, holoprosencephaly, situs inversus syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Agnathia, holoprosencephaly, situs inversus syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus syndrome Finding site Bone structure of mandible false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Agnathia, holoprosencephaly, situs inversus syndrome Finding site Bone structure of mandible true Inferred relationship Existential restriction modifier 1
Agnathia, holoprosencephaly, situs inversus syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Agnathia, holoprosencephaly, situs inversus syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Agnathia, holoprosencephaly, situs inversus syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Agnathia, holoprosencephaly, situs inversus 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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