MYH9-related Disorder(May-Hegglin anomaly) Explore Disorder's Alias
An Autosomal dominant mode(s) within the Blood disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Blood 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 | MYH9/4627 | myosin heavy chain 9 | 22q12.3 | Chr22, NC_000022.11 (36281280..36387967, complement) |
106688 nt | 41 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GARD GTR MedGen MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |