Disease #03971 (MRD21 (mental retardation, autosomal dominant, type 21 (MRD-21)), OMIM:615502)
| Official abbreviation |
MRD21 |
| Name |
mental retardation, autosomal dominant, type 21 (MRD-21) |
| OMIM ID |
615502 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
CTCF |
| Associated tissues |
- |
| Disease features |
microcephaly; thin vermilion border; abnormality of the dentition; hypermetropia, strabismus, delayed dentition; feeding difficulties; congenital cardiopathies; cryptorchidism; hypotonia; global developmental delay, intellectual disability; growth delay; short stature |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-11-30 11:56:35 +01:00 (CET) |
Individuals
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