Disease #04635 (NEDRIHF;MRD31 (neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties), OMIM:616158)
| Official abbreviation |
NEDRIHF;MRD31 |
| Name |
neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties |
| OMIM ID |
616158 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
19 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
PURA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2022-09-15 14:30:32 +02:00 (CEST) |
Individuals
|