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bn:22200452n
Noun Concept
Categories: Autosomal dominant disorders, Syndromes, Transcription factor deficiencies
EN
Emberger syndrome  deafness-lymphedema-leukemia syndrome  Deafness - lymphoedema - leukemia syndrome  LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA
EN
The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. Wikipedia
Definitions
Relations
Sources
EN
The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. Wikipedia
A genetic disorder Wikipedia Disambiguation
IS A
disease
rare disease
head and neck cancer
tumor of hematopoietic and lymphoid tissues
GENETIC ASSOCIATION
GATA2
Wikipedia
EN
Emberger syndrome
Wikidata
EN
Emberger syndrome
Wikidata Alias
EN
deafness-lymphedema-leukemia syndrome, Deafness - lymphoedema - leukemia syndrome, Emberger Syndrome, LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA

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