Disease #00932 (NBS (Nijmegen breakage syndrome (NBS)), OMIM:251260)
| Official abbreviation |
NBS |
| Name |
Nijmegen breakage syndrome (NBS) |
| OMIM ID |
251260 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
16 |
| Phenotype entries for this disease |
15 |
| Associated with 1 gene |
NBN |
| Associated tissues |
- |
| Disease features |
cognitive delay; growth retardation; neuropsychiatric behaviors; microcephaly; craniofacial dysmorphia; cleft/arched palate; syndactyly; organ abnormalitie; no cardiac defects; limb reductions; no hearing loss; skin pigmentation abnormalities; elevated cancer incidence; no bone marrow/hematopoietic defects |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-08-31 23:31:15 +02:00 (CEST) |
Individuals
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