isolated congenital asplenia
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Summary
isolated congenital asplenia is a developmental defect during embryogenesis[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- isolated congenital asplenia's instance of is recorded as developmental defect during embryogenesis[3].
- isolated congenital asplenia's instance of is recorded as rare disease[4].
- isolated congenital asplenia's instance of is recorded as class of disease[5].
- isolated congenital asplenia is a type of asplenia[6].
- isolated congenital asplenia is a type of non-syndromic visceral malformation[7].
- isolated congenital asplenia is a type of other immunodeficiency syndromes due to defects in innate immunity[8].
- isolated congenital asplenia's genetic association is recorded as RPSA[9].
- isolated congenital asplenia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101351[10].
Why It Matters
isolated congenital asplenia is known by 10 alternative names across languages and contexts.[2]