Disease #00574 (del 2q37;BDMR (chromosome deletion syndrome 2q37 (brachydactyly mental retardation syndrome (BDMR))), OMIM:600430)
| Official abbreviation |
del 2q37;BDMR |
| Name |
chromosome deletion syndrome 2q37 (brachydactyly mental retardation syndrome (BDMR)) |
| OMIM ID |
600430 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
HDAC4 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-02-24 17:04:38 +01:00 (CET) |
Individuals
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