Phenotypes for disease #02012 (PCKDC (deficiency, phosphoenolpyruvate carboxykinase, cytosolic (PCKDC)), OMIM:261680)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060491 Phosphoenolpyruvate carboxykinase-1, cytosolic, deficiency (OMIM:261680) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080922
0000070606 mild IDD, transient acute liver failure during viral illness, with episodes of recurrent hyperammonemia, lactic acidosis, elevated tricyclic acid metabolites, stabilization on responsive to carbohydrate rich diet, fatty liver infiltration; recurrent metabolic decompensation - - Familial, autosomal recessive - - - - - Johan den Dunnen 00092270
0000227020 Severe LVOT obstruction LV hypertrophy. Recurrent sub-aortic membrane. Congenital heart valve disease. Congenital heart disease Congenital heart valve disease. Familial, autosomal recessive - 00y10m - congenital - Aida Bertoli-Avella 00299708
0000321817 episodic fasting hypoglycemia, lactic acidemia - PCKDC Familial, autosomal recessive - - - - - Johan den Dunnen 00310676
0000321818 episodic fasting hypoglycemia, lactic acidemia - PCKDC Familial, autosomal recessive - - - - - Johan den Dunnen 00431213
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