Disease #02308 (CPT II deficiency, infantile, OMIM:600649)

Official abbreviation -
Name CPT II deficiency, infantile
OMIM ID 600649
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CPT2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00301524 - - 2 affected sisters F ? Greece - - - - - CPT II deficiency, infantile - CPT2 CPT2 1 2 Helen Latsoudis
00301525 - - 2 affected siblings (1M, 1F) M no Greece - 17y - - - CPT II deficiency, infantile - CPT2 CPT2 1 2 Helen Latsoudis
00305359 162067 - - M ? Germany - - - - - CPT II deficiency, infantile Random finding of a CK elevation (> 12000U/l), no complaints, active in sports, under control CK 2684 U/l; HPO: Abnormality of the musculature DSG2 DSG2 1 1 Andreas Laner
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