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85559002: Pelger-Huët anomaly (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
141810015 Pelger-Huët anomaly en Synonym Active Only initial character case insensitive SNOMED CT core module
141811016 Pelger-Huet anomaly en Synonym Active Entire term case sensitive SNOMED CT core module
827637012 Pelger-Huët anomaly (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1235046013 Pelger Huet anomaly en Synonym Active Only initial character case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pelger-Huët anomaly Is a Genetic anomaly of leukocyte true Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Is a Qualitative abnormality of granulocyte true Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Is a Non-malignant white cell disorder true Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Finding site Leukocyte false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Finding site Entire hematological system false Inferred relationship Existential restriction modifier 1
Pelger-Huët anomaly Associated morphology Pelger-Huët cell false Inferred relationship Existential restriction modifier 1
Pelger-Huët anomaly Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Finding site Structure of immune system false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Has definitional manifestation Pelger-Huët cell false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Associated morphology White blood cell abnormality false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Interprets Laboratory test false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Finding method Procedure false Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Interprets Genetic test true Inferred relationship Existential restriction modifier 2
Pelger-Huët anomaly Is a Pelger-Huët cell true Inferred relationship Existential restriction modifier
Pelger-Huët anomaly Interprets Hematology procedure false Inferred relationship Existential restriction modifier 1
Pelger-Huët anomaly Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 3
Pelger-Huët anomaly Interprets White blood cell test true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome Is a True Pelger-Huët anomaly Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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