OBO ID: DOID:0111092
Term Name: Fanconi anemia complementation group P Search Ontology:
Synonyms:
  • FANCP
Definition: A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3. (2)
References:
Ontology: Human Disease   ( DOID:0111092 )
Relationships
is a type of:
OTHER Fanconi anemia complementation group P PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLX4 Fanconi anemia, complementation group P 613951
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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