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1208488006: Special AT-rich sequence-binding protein 2-associated syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4964841015 SATB2-associated syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4964970011 Special AT-rich sequence-binding protein 2-associated syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
4964971010 Special AT-rich sequence-binding protein 2-associated syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Special AT-rich sequence-binding protein 2-associated syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Is a Developmental delay true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Is a Congenital micrognathism true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Is a Congenital anomaly of tooth true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Special AT-rich sequence-binding protein 2-associated syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Finding site Tooth structure true Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Special AT-rich sequence-binding protein 2-associated syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Special AT-rich sequence-binding protein 2-associated syndrome Finding site Bone structure of mandible true Inferred relationship Existential restriction modifier 2
Special AT-rich sequence-binding protein 2-associated syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Special AT-rich sequence-binding protein 2-associated syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Special AT-rich sequence-binding protein 2-associated syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 3
Special AT-rich sequence-binding protein 2-associated syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Special AT-rich sequence-binding protein 2-associated syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 4
Special AT-rich sequence-binding protein 2-associated syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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