Phenotypes for disease #00394 (HOMG1 (hypomagnesemia 1, intestinal), OMIM:602014)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000015239 initial Mg2+ 0.21 mM, FE Mg2+ 4.8%; age onset 9w - - Isolated (sporadic) - - - seizures - Karl Schlingmann 00016698
0000015240 initial Mg2+ 0.08 mM, FE Mg2+ 2.8%; age onset 3w - - Isolated (sporadic) - - 00y01m seizures - Karl Schlingmann 00016701
0000015241 initial Mg2+ 0.10 mM, FE Mg2+ 4.0% - - Isolated (sporadic) - - 00y04m seizures - Karl Schlingmann 00016705
0000015242 initial Mg2+ 0.41 mM, FE Mg2+high; age onset 4w - - Isolated (sporadic) - - 00y01m seizures - Karl Schlingmann 00016707
0000015243 initial Mg2+ 0.17 mM, FE Mg2+ 4.5%; age onset 5w - - Familial, autosomal recessive - - 00y01m seizures - Karl Schlingmann 00016708
0000015244 initial Mg2+ 0.22 mM, FE Mg2+ 2.6%; age onset 5w - - Familial, autosomal recessive - - 00y01m seizures - Karl Schlingmann 00016843
0000173792 hypomagnesemia (HP:0002917), hypocalcaemia (HP:0002901) HSH HSH Familial, autosomal recessive 05y 05y 00y01m - - John Sayer 00231400
0000306091 Hypomagnesemia, Seizure - - Familial, autosomal recessive - - - - - Andreas Laner 00414236
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