Disease #04460 (NISBD2 (inflammatory skin and bowel disease, neonatal, type 2 (NISBD-2)), OMIM:616069)
Official abbreviation |
NISBD2 |
Name |
inflammatory skin and bowel disease, neonatal, type 2 (NISBD-2) |
OMIM ID |
616069 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
EGFR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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