Table B.

OMIM Entries for NR0B1-Related Adrenal Hypoplasia Congenita (View All in OMIM)

300143INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 21; XLID21
300200ADRENAL HYPOPLASIA, CONGENITAL; AHC
300206INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN-LIKE 1; IL1RAPL1
300377DYSTROPHIN; DMD
300473NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
300474GLYCEROL KINASE; GK
307030GLYCEROL KINASE DEFICIENCY; GKD
310200MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD

From: NR0B1-Related Adrenal Hypoplasia Congenita

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