Disease #00166 (NBSLD (Nijmegen breakage syndrome-like disorder (NBSLD)), OMIM:613078)
Official abbreviation |
NBSLD |
Name |
Nijmegen breakage syndrome-like disorder (NBSLD) |
OMIM ID |
613078 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
RAD50 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-07-21 20:24:30 +02:00 (CEST) |
Date last edited |
2016-03-20 12:13:59 +01:00 (CET) |
Individuals
|
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