Phenotypes for disease #05195 (HCINF2 (hypercalcemia, infantile, type 2 (HCINF-2)), OMIM:616963)

17 entries on 1 page. Showing entries 1 - 17.
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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     
0000073558 diagnosis infantile hypercalcemia; ephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148), Hypoparathyroidism (HP:0000829), Increased serum 1,25-dihydroxyvitamin D3 (HP:0003152) - - Familial, autosomal recessive 00y02m - - - - Pieter Klap 00074404
0000073559 diagnosis infantile hypercalcemia; failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), no muscular hypotonia (-HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148) - - Familial, autosomal recessive 00y02m - - - - Johan den Dunnen 00074405
0000073560 Failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), Muscular hypotonia (HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148), Hypoparathyroidism (HP:0000829), Increased serum 1,25-dihydroxyvitamin D3 (HP:0003152), - - Familial, autosomal recessive <00y01m - <00y01m failure to thrive (HP:0001508) - Pieter Klap 00074402
0000073561 failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), no muscular hypotonia (-HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148) - - Familial, autosomal recessive 00y01m - 00y01m failure to thrive (HP:0001508) - Pieter Klap 00074403
0000073562 see paper; … - - Familial, autosomal recessive 14y - 2m - - Johan den Dunnen 00095161
0000073563 see paper; … - - Unknown 10y - 4m - - Johan den Dunnen 00095162
0000073564 see paper; … - - Unknown 17y - 9m - - Johan den Dunnen 00095163
0000073565 see paper; … - - Familial, autosomal recessive 3y - 10m - - Johan den Dunnen 00095164
0000073566 see paper; … - - Familial, autosomal recessive 3y - 1m - - Johan den Dunnen 00095165
0000073567 see paper; … - - Familial, autosomal recessive 11m - 3m - - Johan den Dunnen 00095166
0000073568 see paper; … - - Familial, autosomal recessive 1y - 3m - - Johan den Dunnen 00095167
0000073569 see paper; … - - Familial, autosomal recessive 11m - 4m - - Johan den Dunnen 00095168
0000073570 see paper; … - - Familial, autosomal recessive 11y - 7m - - Johan den Dunnen 00095169
0000073571 see paper; … - - Unknown 6y - 6m - - Johan den Dunnen 00095170
0000073572 see paper; … - - Familial, autosomal recessive 1y - 3m - - Johan den Dunnen 00095171
0000073573 see paper; … - - Familial, autosomal recessive 3y6m - 1y6m - - Johan den Dunnen 00095172
0000187182 Nephrocalcinosis, Muscular hypotonia, Failure to thrive - - Familial, autosomal recessive - - - - - Valeriia Apukhtina 00248174
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