Disease #02528 (CORTRD1 (cortisone reductase deficiency, type 1 (CORTRD-1)), OMIM:604931)

Official abbreviation CORTRD1
Name cortisone reductase deficiency, type 1 (CORTRD-1)
OMIM ID 604931
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene H6PD
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

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00092240 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F - United States - - - - - CORTRD1, Krabbe congenital hypotonia, respiratory/feeding insufficiency, IDD secondary to myopathy, premature adrenarche, skin pigmentation abnormalities; transient glycogen storage on muscle biopsy GALC, H6PD GALC 1 1 Johan den Dunnen
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