Maternal uniparental disomy of chromosome 9

Orpha code: 96183OMIM code:

Definicja

Maternal uniparental disomy of chromosome 9 is a uniparental disomy of maternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only mother is a carrier.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
UPD(9)mat
UPD(9)mat
Kod ORPHA
96183
Kod OMIM
-
Kod ICD10
Q99.8
Kod ICD11
-

No additional description.

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