Fanconi anemia complementation group B
Fanconi anemia that has material basis in mutation in the FANCB gene on chromosome Xp22
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Summary
Fanconi anemia complementation group B is a rare disease[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- Fanconi anemia complementation group B's instance of is recorded as rare disease[3].
- Fanconi anemia complementation group B's instance of is recorded as class of disease[4].
- Fanconi anemia complementation group B is a type of Fanconi anemia[5].
- Fanconi anemia complementation group B is a type of genetic disease[6].
- Fanconi anemia complementation group B is a type of X-linked recessive disease[7].
- Fanconi anemia complementation group B's NCI Thesaurus ID is recorded as C125703[8].
- Fanconi anemia complementation group B's genetic association is recorded as FANCB[9].
- Fanconi anemia complementation group B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111098[10].
- Fanconi anemia complementation group B's exact match is recorded as http://identifiers.org/doid/DOID:0111098[11].
- Fanconi anemia complementation group B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_84[12].
- Fanconi anemia complementation group B's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
Fanconi anemia complementation group B is known by 10 alternative names across languages and contexts.[2]