Disease #00349 (CFID (deficiency, complement factor I), OMIM:610984)

Official abbreviation CFID
Name deficiency, complement factor I
OMIM ID 610984
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CFI
Associated tissues -
Disease features -
Remarks -
Date created 2014-03-13 09:55:00 +01:00 (CET)
Date last edited 2025-03-26 19:40:48 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00464538 - - - F yes Iran - - - - - CFID Recurrent infections CFI CFI 1 1 Nima Parvaneh
00464539 - - - F yes Iran - - - - - CFID Recurrent infections CFI CFI 1 1 Nima Parvaneh
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