Phenotypes for disease #04103 (AGS7 (Aicardi-Goutieres syndrome, type 7 (AGS7)), OMIM:615846)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000087492 Initially normal development, regression, severe ID, spasticity, scoliosis, episodic icterus and skin swelling - - Familial, autosomal dominant - - - - - Bernt Popp 00111407
0000127742 Spasticity and intracranial calcification - - Familial, autosomal dominant - - - Spasticity and intracranial calcification - Yanick Crow 00155022
0000270741 overlaps with Singleton-Merten syndrome type 1 - - Isolated (sporadic) - - - - - Kosei Hasegawa 00375514
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