Preferred Name |
Caspase-8 deficiency |
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Synonyms |
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Definitions |
(CASP8D): Disorder resembling autoimmune lymphoproliferative syndrome (ALPS). It is characterized by lymphadenopathy, splenomegaly, and defective CD95-induced apoptosis of peripheral blood lymphocytes (PBLs). It leads to defects in activation of T-lymphocytes, B-lymphocytes, and natural killer cells leading to immunodeficiency characterized by recurrent sinopulmonary and herpes simplex virus infections and poor responses to immunization. |
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ID |
http://purl.obolibrary.org/obo/OMIM_607271 |
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definition |
(CASP8D): Disorder resembling autoimmune lymphoproliferative syndrome (ALPS). It is characterized by lymphadenopathy, splenomegaly, and defective CD95-induced apoptosis of peripheral blood lymphocytes (PBLs). It leads to defects in activation of T-lymphocytes, B-lymphocytes, and natural killer cells leading to immunodeficiency characterized by recurrent sinopulmonary and herpes simplex virus infections and poor responses to immunization. |
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has_obo_namespace |
cell_cycle_ontology |
|
id |
OMIM:607271 |
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label |
Caspase-8 deficiency |
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notation |
OMIM:607271 |
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prefLabel |
Caspase-8 deficiency |
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treeView | ||
subClassOf |
Delete | Mapping To | Ontology | Source |
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http://nanbyodata.jp/ontology/NANDO_2200740 | NANDO | LOOM | |
http://identifiers.org/omim/607271 | REXO | LOOM | |
http://identifiers.org/omim/607271 | GEXO | LOOM | |
http://identifiers.org/omim/607271 | RETO | LOOM | |
http://purl.bioontology.org/ontology/OMIM/607271 | OMIM | LOOM |