bn:02255036n
Noun Concept
Categories: Genetic disorders, Autosomal monosomies and deletions
EN
2q37 monosomy  Albright Hereditary Osteodystrophy-Like Syndrome  Albright hereditary osteodystrophy type 3  BDMR  Brachydactyly-intellectual disability syndrome
EN
2q37 monosomy is a rare genetic disorder caused by a deletion of a segment at the end of chromosome 2. Wikipedia
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