Mondo Disease Ontology
2296 terms(s) returned
| Term Type: | Record: 2101 to 2150 of 2296 Records | Page: 43 of 46, First Previous Next Last | Show Records Per Page |
- is allocated id range
- is basis for realizable
- is causal gain of function germline mutation of in
- is causal germline mutation in
- is causal somatic mutation in
- is denotator type
- is deprotonated form of
- is enantiomer of
- is genetic basis for condition
- is kinase activity
- is protonated form of
- is substitutent group from
- is tautomer of
- isReferencedBy
- is_class_level
- is_metadata_tag
- ischemia reperfusion injury
- ischemic bowel disorder
- ischemic colitis
- ischemic disease
- ischemic fasciitis
- ischemic myopathy, non-human animal
- ischemic neuropathy
- ischemic stroke
- ischial cartilage element
- ischial endochondral element
- ischial pre-cartilage condensation
- ischio-vertebral syndrome
- ischium
- islet cell adenomatosis
- islet of Langerhans
- isoalloxazine
- isobutane
- isobutyl group
- isobutyryl-CoA dehydrogenase deficiency
- isochromosome Y
- isochromosomy Yp
- isochromosomy Yq
- isocyanate induced asthma
- isocyanates
- isocyanic acid
- isolated Dandy-Walker malformation with hydrocephalus
- isolated Dandy-Walker malformation without hydrocephalus
- isolated Pierre-Robin syndrome
- isolated adrenal insufficiency
- isolated agammaglobulinemia
- isolated agenesis of gallbladder
- isolated amyelia
- isolated anal canal duplication
- isolated anencephaly
