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1208342001: Eye defects, arachnodactyly, cardiopathy 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
4963741017 Eye defects, arachnodactyly, cardiopathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4963742012 Al Gazali Al Talabani syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4963743019 Eye defects, arachnodactyly, cardiopathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4963744013 Al Gazali Lytle 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
Eye defects, arachnodactyly, cardiopathy syndrome Is a Dysostosis true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Congenital anomaly of anterior segment of eye true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Heart disease true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Congenital cardiovascular disorder true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Eye defects, arachnodactyly, cardiopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Eye defects, arachnodactyly, cardiopathy syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Eye defects, arachnodactyly, cardiopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Eye defects, arachnodactyly, cardiopathy syndrome Finding site Anterior eyeball segment structure true Inferred relationship Existential restriction modifier 2
Eye defects, arachnodactyly, cardiopathy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Eye defects, arachnodactyly, cardiopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Eye defects, arachnodactyly, cardiopathy syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Eye defects, arachnodactyly, cardiopathy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Eye defects, arachnodactyly, cardiopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Eye defects, arachnodactyly, cardiopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Eye defects, arachnodactyly, cardiopathy syndrome Finding site Heart structure true Inferred relationship Existential restriction modifier 5
Eye defects, arachnodactyly, cardiopathy syndrome Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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