DOCK2 deficiency
human disease
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DOCK2 deficiency
Summary
DOCK2 deficiency is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- DOCK2 deficiency's instance of is recorded as rare disease[3].
- DOCK2 deficiency's instance of is recorded as class of disease[4].
- DOCK2 deficiency is a type of non-severe combined immunodeficiency[5].
- DOCK2 deficiency is a type of autosomal recessive disease[6].
- DOCK2 deficiency is a type of combined immunodeficiency[7].
- DOCK2 deficiency's genetic association is recorded as DOCK2[8].
- DOCK2 deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_447737[9].
- DOCK2 deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111951[10].
- DOCK2 deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111951[11].
Why It Matters
DOCK2 deficiency is known by 5 alternative names across languages and contexts.[2]