Chromosome inversion in normal individual

Description

Any disease caused by inversion of genetic material on a chromosome, in an individual demonstrating no abnormalities. Confirmation is through observation of a chromosomal inversion by genetic testing.

Index terms

Chromosome inversion in normal individual

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LD47.0 – Balanced translocation and insertion in normal individual
LD47.2 – Balanced autosomal rearrangement in abnormal individual
LD47.3 – Balanced sex or autosomal rearrangement in abnormal individual
LD47.4 – Autosomal fragile site
LD47.Y – Other specified balanced rearrangements or structural rearrangements
LD47.Z – Balanced rearrangements or structural rearrangements, unspecified

Foundation entity

Chromosome inversion in normal individual – http://id.who.int/icd/entity/1635052482

Part of: LD47: Balanced rearrangements or structural rearrangements › 20: Developmental anomalies