FAM72D
Description
The FAM72D (family with sequence similarity 72 member D) is a protein-coding gene located on chromosome 1.
FAM72D is also known as GCUD2.
Associated Diseases
- familial juvenile hyperuricemic nephropathy type 1
- common variable immunodeficiency
- combined immunodeficiency with skin granulomas
- BENTA disease
- multicystic dysplastic kidney
- karyomegalic interstitial nephritis
- severe combined immunodeficiency due to CTPS1 deficiency
- immunodeficiency 18
- xanthinuria type II
- hypoxanthine guanine phosphoribosyltransferase partial deficiency
- immunodeficiency 62
- immunodeficiency, common variable, 14
- hyper-IgM syndrome type 3
- hypouricemia, renal, 2
- infundibulopelvic stenosis-multicystic kidney syndrome
- immunodeficiency 105
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
- familial juvenile hyperuricemic nephropathy type 2
