Pages that link to "Property:P409"
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The following pages link to exact match (P409):
Displaying 50 items.
- genetic biliary tract disease (Q17575) (← links)
- rare genetic hepatic disease (Q17576) (← links)
- rare genetic endocrine disease (Q17577) (← links)
- rare genetic gastroenterological disease (Q17578) (← links)
- HFE hereditary haemochromatosis (Q17579) (← links)
- iron metabolism disease (Q17581) (← links)
- mineral metabolism disease (Q17582) (← links)
- disorder of metabolite absorption and transport (Q17583) (← links)
- inherited metabolic disorder (Q17586) (← links)
- metal metabolism disorder (Q17587) (← links)
- Wilson disease (Q17588) (← links)
- copper metabolism disease (Q17589) (← links)
- rare hereditary metabolic disease with peripheral neuropathy (Q17590) (← links)
- metabolic disease with cataract (Q17591) (← links)
- metabolic disease associated with ocular features (Q17592) (← links)
- rare genetic eye disease (Q17593) (← links)
- rare eye disease (Q17594) (← links)
- propionate-CoA ligase activity (Q17596) (← links)
- metabolic disease with corneal opacity (Q17597) (← links)
- corneal opacity (Q17598) (← links)
- corneal disease (Q17599) (← links)
- 2-methylcitrate synthase activity (Q17602) (← links)
- cornea symptom (Q17603) (← links)
- propionyl-CoA C2-trimethyltridecanoyltransferase activity (Q17604) (← links)
- supranuclear oculomotor palsy (Q17605) (← links)
- propionyl-CoA:succinate CoA-transferase activity (Q17606) (← links)
- rare genetic tremor disorder (Q17607) (← links)
- genetic movement disorder (Q17608) (← links)
- 2-oxobutyrate synthase activity (Q17609) (← links)
- rare metabolic liver disease (Q17610) (← links)
- acryloyl-CoA reductase (NADP+) activity (Q17611) (← links)
- metal transport or utilization disorder with epilepsy (Q17612) (← links)
- metabolic diseases with epilepsy (Q17613) (← links)
- 2-ketobutyrate formate-lyase activity (Q17614) (← links)
- rare genetic epilepsy (Q17615) (← links)
- propionyl-CoA metabolic process (Q17616) (← links)
- neurometabolic disease (Q17617) (← links)
- propionyl-CoA catabolic process (Q17618) (← links)
- rare disorder with dystonia and other neurologic or systemic manifestation (Q17619) (← links)
- rare genetic dystonia (Q17620) (← links)
- dystonia (Q17622) (← links)
- propionyl-CoA biosynthetic process (Q17623) (← links)
- nephropathy secondary to a storage or other metabolic disease (Q17624) (← links)
- rare genetic renal disease (Q17625) (← links)
- kidney disease (Q17626) (← links)
- 5-dehydro-2-deoxyphosphogluconate aldolase activity (Q17628) (← links)
- 3-aci-nitropropanoate oxidase activity (Q17631) (← links)
- oxidoreductase activity, acting on other nitrogenous compounds as donors, oxygen as acceptor (Q17632) (← links)
- edema (Q17633) (← links)
- acetylenecarboxylate hydratase activity, producing 3-oxopropanoate (Q17634) (← links)