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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