Disease #01080 (HSAS (hydrocephalus, with congenital stenosis of aqueduct of Sylvis (HSAS, hydrocephalus with Hirschsprung disease)), OMIM:307000)
| Official abbreviation |
HSAS |
| Name |
hydrocephalus, with congenital stenosis of aqueduct of Sylvis (HSAS, hydrocephalus with Hirschsprung disease) |
| OMIM ID |
307000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
L1CAM |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-09-08 13:29:04 +02:00 (CEST) |
Individuals
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