Disease #01872 (CIP;HSAN2D (pain, indifference, congenital, autosomal recessive (CIP)), OMIM:243000)
| Official abbreviation |
CIP;HSAN2D |
| Name |
pain, indifference, congenital, autosomal recessive (CIP) |
| OMIM ID |
243000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
17 |
| Phenotype entries for this disease |
15 |
| Associated with 1 gene |
SCN9A |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-01-10 16:00:14 +01:00 (CET) |
Individuals
|