Uniparental disomies of paternal origin

Description

Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.

Index terms

Uniparental disomies of paternal origin
Paternal uniparental disomy of chromosome 1
Paternal uniparental disomy of chromosome 4

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Paternal uniparental disomy of chromosome 5
Paternal uniparental disomy of chromosome 6
Paternal uniparental disomy of chromosome 7
Paternal uniparental disomy of chromosome 11
Paternal uniparental disomy of chromosome 13
Paternal uniparental disomy of chromosome 14
Paternal uniparental disomy of chromosome 15
Paternal uniparental disomy of chromosome 20
Paternal uniparental disomy of chromosome 21
Paternal uniparental disomy of chromosome X

Exclusions from above levels

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

Sibling codes

LD45.0 – Uniparental disomies of maternal origin
LD45.Y – Other specified uniparental disomies
LD45.Z – Uniparental disomies, unspecified

Foundation entity

Uniparental disomies of paternal origin – http://id.who.int/icd/entity/2028476598

Part of: LD45: Uniparental disomies › 20: Developmental anomalies