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722127006: Pacman dysplasia (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
3330822017 Pacman dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330823010 Pacman dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3330824016 Epiphyseal stippling with osteoclastic hyperplasia 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
Pacman dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Pacman dysplasia Is a Osteolysis true Inferred relationship Existential restriction modifier
Pacman dysplasia Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier
Pacman dysplasia Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Pacman dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Pacman dysplasia Associated morphology Osteolysis true Inferred relationship Existential restriction modifier 1
Pacman dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pacman dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Pacman dysplasia Is a Congenital disease 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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