Kidney Tissue Atlas Ontology
11852 terms(s) returned
| Term Type: | Record: 701 to 750 of 11852 Records | Page: 15 of 238, First Previous Next Last | Show Records Per Page |
- Beckwith-Wiedemann syndrome due to 11p15 microdeletion
- Beckwith-Wiedemann syndrome due to 11p15 microduplication
- Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
- Beckwith-Wiedemann syndrome due to CDKN1C mutation
- Beckwith-Wiedemann syndrome due to NSD1 mutation
- Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
- Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
- Beemer-Langer syndrome
- Behavioral abnormality
- Behcet disease
- Belkofski
- Benzothiadiazines [Chemical/Ingredient]
- Benzylisoquinolines [Chemical/Ingredient]
- Bering Straits Inupiat
- Betapolyomavirus
- Bethel
- Bhutanese
- Bicarbonate-wasting renal tubular acidosis
- Bicyclo Compounds [Chemical/Ingredient]
- Bicyclo Compounds, Heterocyclic [Chemical/Ingredient]
- Big Cypress
- Bilateral fetal pyelectasis
- Bilateral renal agenesis
- Bilateral renal atrophy
- Bilateral renal dysplasia
- Bilateral renal hypoplasia
- Bilateria
- Bill Moore's Slough
- Biloxi
- Binucleated visceral epithelial cells
- Biogenic Amines [Chemical/Ingredient]
- Biogenic Monoamines [Chemical/Ingredient]
- Biological Factors [Chemical/Ingredient]
- Biological Macromolecular Activity [MoA]
- Birch Creek
- Birt-Hogg-Dube syndrome
- Birth Weight (NCIT)
- Bishop
- Black
- Black Central American
- Black South American
- Black South or Central American
- Black or African American
- Blackfeet
- Blackfoot Sioux
- Blebbing of apical cytoplasm of renal tubular epithelial cells
- Blindness
- Blood & Lymphatic Fluid Function Alteration [PE]
- Blood Coagulation Disorders [Disease/Finding]
- Blood Coagulation Disorders, Inherited [Disease/Finding]
