Pages that link to "Property:P1"
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The following pages link to subclass of (P1):
Displaying 50 items.
- ascending cholangitis (Q17567) (← links)
- non-neoplastic bile duct disorder (Q17568) (← links)
- bile duct disease (Q17569) (← links)
- biliary tract disease (Q17570) (← links)
- biliary disease (Q17571) (← links)
- bile ducts (Q17572) (← links)
- duct (Q17573) (← links)
- segment of biliary tree (Q17574) (← links)
- 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 overload (Q17580) (← links)
- iron metabolism disease (Q17581) (← links)
- mineral metabolism disease (Q17582) (← links)
- overload disease (Q17585) (← links)
- inherited metabolic disorder (Q17586) (← links)
- metal metabolism disorder (Q17587) (← links)
- Wilson disease (Q17588) (← links)
- copper metabolism disease (Q17589) (← 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)
- hereditary eye disease (Q17595) (← links)
- propionate-CoA ligase activity (Q17596) (← links)
- metabolic disease with corneal opacity (Q17597) (← links)
- corneal opacity (Q17598) (← links)
- corneal disease (Q17599) (← links)
- cornea (Q17600) (← links)
- fibrous tunic of eyeball (Q17601) (← links)
- 2-methylcitrate synthase activity (Q17602) (← links)
- cornea symptom (Q17603) (← links)
- propionyl-CoA C2-trimethyltridecanoyltransferase activity (Q17604) (← 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)