Disease #07004 (NEDHFS (neurodevelopmental disorder with hypotonia, dysmorphic facies, skin abnormalities), OMIM:620191)
| Official abbreviation |
NEDHFS |
| Name |
neurodevelopmental disorder with hypotonia, dysmorphic facies, skin abnormalities |
| OMIM ID |
620191 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PGM2L1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-02-08 20:03:36 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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