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Q35196912-7B9DE78A-BCBF-4EDC-BF7B-1CB9B092CC5E
Q35196912-7B9DE78A-BCBF-4EDC-BF7B-1CB9B092CC5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196912-7B9DE78A-BCBF-4EDC-BF7B-1CB9B092CC5E
Homozygosity for a newly identified missense mutation in a patient with very severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID).
P2860
Q35196912-7B9DE78A-BCBF-4EDC-BF7B-1CB9B092CC5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196912-7B9DE78A-BCBF-4EDC-BF7B-1CB9B092CC5E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
647dad1bd8f0b36610bcf5edb6f21e6bd18e5110
P2860
The chondro-osseous dysplasia of adenosine deaminase deficiency with severe combined immunodeficiency.