Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B035b3072f1cb480bed07c7ccd6a762d6> ?p ?o ?g. }
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- B035b3072f1cb480bed07c7ccd6a762d6 hasDbXref "NCIT:C98898" @default.
- B035b3072f1cb480bed07c7ccd6a762d6 type Axiom @default.
- B035b3072f1cb480bed07c7ccd6a762d6 annotatedProperty IAO_0000115 @default.
- B035b3072f1cb480bed07c7ccd6a762d6 annotatedSource MONDO_0018963 @default.
- B035b3072f1cb480bed07c7ccd6a762d6 annotatedTarget "Methemoglobinemia inherited in an autosomal recessive pattern. It is caused by deficiency of the enzyme NADH methemoglobin reductase or the presence of abnormal hemoglobin M. It presents with cyanosis early in life. There is no evidence of cardiopulmonary disease present." @default.