Disease #05215 (nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency)

Official abbreviation -
Name nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency
OMIM ID -
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SGPL1
Associated tissues -
Disease features -
Remarks -
Date created 2017-01-13 21:44:48 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095243 - - - M yes - European - - - hemodialysis, total parenteral nutrition, cortisol supplementation nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency congenital nephrotic syndrome associated with male hypergonadotropic hypogonadism and with adrenal calcification with and without adrenal insufficiency - SGPL1 1 1 Andreas Janecke
00095244 - - - M yes - Arab 00y03m - - - nephrotic syndrome, congenital, male hypergonadotropic hypogonadism, adrenal calcification with/without adrenal insufficiency congenital nephrotic syndrome associated with male hypergonadotropic hypogonadism and with adrenal calcification with and without adrenal insufficiency - SGPL1 1 1 Andreas Janecke
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