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- B9f83c386e6b2f94de5d92ff029b4174c hasDbXref "https://rarediseases.info.nih.gov/diseases/1218/neuronal-ceroid-lipofuscinosis-10" @default.
- B9f83c386e6b2f94de5d92ff029b4174c type Axiom @default.
- B9f83c386e6b2f94de5d92ff029b4174c annotatedProperty IAO_0000115 @default.
- B9f83c386e6b2f94de5d92ff029b4174c annotatedSource MONDO_0012414 @default.
- B9f83c386e6b2f94de5d92ff029b4174c annotatedTarget "A rare condition that affects the nervous system. Signs and symptoms of the condition can develop any time from birth to adulthood and may include progressive dementia, seizures, lack of muscle coordination, and vision loss. CLN10-NCL is caused by changes (mutations) in the CTSD gene and is inherited in an autosomal recessive manner. Treatment options are limited to therapies that can help relieve some of the symptoms." @default.