Phenotypes for disease #00980 (hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH), OMIM:238970)

15 entries on 1 page. Showing entries 1 - 15.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000088104 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00112540
0000088105 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00112541
0000088106 3.5y first speech problems; 6y hospitalized for first attack with severe tantrum, confusion, gait disturbances, loss of speech abilities, physical examination showed upward paralysis, aphasia, bilateral flask paralysis upper/lower extremities and deep tendon reflexes. Cranial CT, MRI, EMG and fundoscopic findings were normal; intolerance for protein-rich foods, presented hyperornithinemia, hyperammonemia, homocitrullinuria - - Familial, autosomal recessive - - - - - Nagehan Ersoy Tunali 00112542
0000088107 - - - Unknown - - - - - Johan den Dunnen 00112543
0000088108 - - - Unknown - - - - - Johan den Dunnen 00112544
0000088110 - - - Unknown - - - - - Johan den Dunnen 00112546
0000088113 - - - Unknown - - - - - Johan den Dunnen 00112549
0000088114 - - - Unknown - - - - - Johan den Dunnen 00112550
0000088115 - - - Unknown - - - - - Johan den Dunnen 00112551
0000088117 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00112553
0000088118 - - - Unknown - - - - - Johan den Dunnen 00112554
0000088122 - - - Unknown - - - - - Johan den Dunnen 00112558
0000088123 - - - Unknown - - - - - Johan den Dunnen 00112559
0000088124 - - - Unknown - - - - - Johan den Dunnen 00112560
0000340122 Seizures, hyperammonemia, intellectual disability, abnormality of coagulation Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome Familial, autosomal recessive - 00y00m01d - - - Miriam Erandi Reyna-Fabián 00451367
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