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
|