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
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