Version: 8.0.0
Date: Tue Jan 28 2025
2 results
Disease Genes: GREB1L (Hsa)

renal agenesis

Disease
Source: DOID:14766
Definition: A renal disease that is characterized by the failure of one or both kidneys to develop.
Genes: GREB1L (Hsa)

autosomal dominant nonsyndromic deafness 80

Disease
Source: DOID:0070602
Definition: An autosomal dominant nonsyndromic deafness characterized by congenital deafness associated with absent or malformed cochleae and eighth cranial nerves that has_material_basis_in heterozygous mutation in the GREB1L gene on chromosome 18q11.
Genes: GREB1L (Hsa)