Disease #05918 (IDDSAPN (intellectual developmental disorder, speech delay, axonal peripheral neuropathy (IDDSAPN)), OMIM:619099)
| Official abbreviation |
IDDSAPN |
| Name |
intellectual developmental disorder, speech delay, axonal peripheral neuropathy (IDDSAPN) |
| OMIM ID |
619099 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NEMF |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-04-07 09:02:06 +02:00 (CEST) |
| Date last edited |
N/A |
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