Disease #00188 (NBS (NIJMEGEN BREAKAGE SYNDROME), OMIM:251260)

Official abbreviation NBS
Name NIJMEGEN BREAKAGE SYNDROME
OMIM ID 251260
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NBN
Associated tissues -
Disease features -
Remarks -
Date created 2023-07-17 13:35:06 +00:00 (UTC)
Date last edited N/A

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