FAM83H - Gene browser | 3billion

FAM83H

FAM83H

family with sequence similarity 83 member H

HCNC Approved Symbol: FAM83H (HGNC:24797)
Genomic Coordinates: 8:143,723,933 - 143,733,779 (8q24.3)
Synonyms: FLJ46072
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the FAM83H gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

02
Patient count

Amelogenesis imperfecta: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

FAM83H - Gene browser | 3billion