Disease #07142 (NEDHBA (neurodevelopmental disorder with hypotonia and characteristic brain abnormalities), OMIM:620746)
| Official abbreviation |
NEDHBA |
| Name |
neurodevelopmental disorder with hypotonia and characteristic brain abnormalities |
| OMIM ID |
620746 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC4A10 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-12-18 15:46:43 +01:00 (CET) |
| Date last edited |
N/A |
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