Polyploidies

Description

Any disease caused by one or more additional sets of chromosomes. Non-mosaic versions of these diseases are characterised by gross fetal malformation or death of the fetus. Confirmation is through observation of supernumerary sets of chromosomes by karyotyping.

Exclusions from above levels

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

Child codes

LD42.0 – Triploidy
LD42.1 – Tetraploidy
LD42.Y – Other specified polyploidies
LD42.Z – Polyploidies, unspecified

Sibling codes

LD40 – Complete trisomies of the autosomes
LD41 – Duplications of the autosomes
LD43 – Complete monosomies of the autosomes
LD44 – Deletions of the autosomes
LD45 – Uniparental disomies
LD46 – Imprinting errors
LD47 – Balanced rearrangements or structural rearrangements
LD7Y – Other specified chromosomal anomalies, excluding gene mutations
LD7Z – Chromosomal anomalies, excluding gene mutations, unspecified

Foundation entity

Polyploidies – http://id.who.int/icd/entity/1286128770

Part of: 20: Developmental anomalies