Disease #06648 (AMC2 (arthrogryposis multiplex congenita, type 2, neurogenic), OMIM:208100)
| Official abbreviation |
AMC2 |
| Name |
arthrogryposis multiplex congenita, type 2, neurogenic |
| OMIM ID |
208100 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ERGIC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2024-10-01 09:43:19 +02:00 (CEST) |
Individuals
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