Hyperphosphatasia with Mental Retardation Syndrome 1 (*)

Alternative Names

  • HPMRS1
  • Mabry Syndrome
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Other congenital malformations

OMIM Number

239300

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1p36.11

Epidemiology in the Arab World

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