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724226009: Infantile osteopetrosis with neuroaxonal dysplasia 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
3437863010 Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3437864016 Infantile osteopetrosis with neuroaxonal dysplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3437865015 Infantile osteopetrosis with neuroaxonal dysplasia 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
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Osteopetrosis true Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Agenesis of corpus callosum true Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Finding site Entire corpus callosum false Inferred relationship Existential restriction modifier 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Finding site Entire corpus callosum true Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Associated morphology Agenesis true Inferred relationship Existential restriction modifier 2
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a Chronic brain syndrome true Inferred relationship Existential restriction modifier
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Interprets Osteoclast turnover rate true Inferred relationship Existential restriction modifier 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Clinical course Progressive 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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