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OMIM ID
267500
OMIM term:
RETICULAR DYSGENESIS
Alternative terms:
RETICULAR DYSGENESIA
CONGENITAL ALEUKIA
SEVERE COMBINED IMMUNODEFICIENCY WITH LEUKOPENIA
DE VAAL DISEASE
HEMATOPOIETIC HYPOPLASIA, GENERALIZED
ALEUKOCYTOSIS
(∗) Location:
1p35.1
(†) Associated OMIM genes:
AK2
(‡) Associated MGI genes:
Mouse
Zebrafish
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