Disease #06213 (NEDHILD;MRD40 (neurodevelopmental disorder with hypotonia, impaired language, dysmorphic features (MRD40)), OMIM:616579)
| Official abbreviation |
NEDHILD;MRD40 |
| Name |
neurodevelopmental disorder with hypotonia, impaired language, dysmorphic features (MRD40) |
| OMIM ID |
616579 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CHAMP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2023-10-23 16:08:01 +02:00 (CEST) |
Individuals
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