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DOID:0112254 - hepatic venoocclusive disease with immunodeficiency
Disease Ontology Definition:A syndrome characterized by severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells, hepatic vascular occlusion, and fibrosis that has_material_basis_in homozygous or compound heterozygous mutation in the SP110 gene on chromosome 2q37.1.
Synonyms: hepatic veno-occlusive disease-immunodeficiency syndrome, VODI
Xenbase Genes
:
sp110
| MIM:235550 - HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY; VODI |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)