Disease #00375 (NPHP13 (nephronophthisis, type 13 (NPHP-13)), OMIM:614377)
Official abbreviation |
NPHP13 |
Name |
nephronophthisis, type 13 (NPHP-13) |
OMIM ID |
614377 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
WDR19 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-05-02 09:58:44 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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