Ramon Syndrome(Gingival fibromatosis combined with cherubism) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Oral disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Oral disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | ELMO2/63916 | engulfment and cell motility 2 | 20q13.12 | Chr20, NC_000020.11 (46366050..46406615, complement) |
40566 nt | 22 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GARD GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |