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1237618009: Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5100058012 SOPH (short stature, optic nerve atrophy, Pelger-Huët anomaly) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5100059016 Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5100060014 Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Short stature disorder true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Inherited optic neuropathy true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Hereditary white blood cell disorder true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Congenital atrophy of optic nerve true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Pelger-Huët anomaly true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Interprets White blood cell test true Inferred relationship Existential restriction modifier 6
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Interprets Genetic test true Inferred relationship Existential restriction modifier 7
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Interprets Body height measure true Inferred relationship Existential restriction modifier 5
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 5
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Finding site Leukocyte true Inferred relationship Existential restriction modifier 4
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Pathological process Abnormal immune process 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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