Congenital Microvillous Atrophy(Davidson disease) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Gastrointestinal disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Gastrointestinal 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 | MYO5B/4645 | myosin VB | 18q21.1 | Chr18, NC_000018.10 (49822789..50195147, complement) |
372359 nt | 40 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
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Clinical Symptoms & Disabilities