Disease #05960 (NEDHYMS (neurodevelopmental disorder with hypotonia, microcephaly, and seizures (NEDHYMS)), OMIM:618862)
Official abbreviation |
NEDHYMS |
Name |
neurodevelopmental disorder with hypotonia, microcephaly, and seizures (NEDHYMS) |
OMIM ID |
618862 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ADARB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-07-28 16:29:00 +02:00 (CEST) |
Date last edited |
N/A |
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