Kidney Tissue Atlas Ontology
2185 terms(s) returned
| Term Type: | Record: 51 to 100 of 2185 Records | Page: 2 of 44, First Previous Next Last | Show Records Per Page |
- Bardet-Biedl syndrome 6
- Bardet-Biedl syndrome 7
- Bardet-Biedl syndrome 8
- Bardet-Biedl syndrome 9
- Bartter disease type 1
- Bartter disease type 2
- Bartter disease type 3
- Bartter disease type 4B
- Bartter disease type 4a
- Bartter disease type 5
- Bartter syndrome
- Bartter syndrome with hypocalcemia
- Beckwith-Wiedemann syndrome
- 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
- Behcet disease
- Birt-Hogg-Dube syndrome
- Braddock syndrome
- Bunyaviridae infectious disease
- C1q nephropathy
- C3 glomerulonephritis
- CHARGE syndrome
- COL4A1 or COL4A2-related cerebral small vessel disease
- COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendancy
- CREST syndrome
- Cerebrorenodigital syndrome
- Charcot-Marie-Tooth disease
- Charcot-Marie-Tooth disease dominant intermediate E
- Crouzon syndrome-acanthosis nigricans syndrome
- Cryoglobulinemic vasculitis
- Cushing syndrome
- DNA repair disease
- Deal Barratt Dillon syndrome
- Dent disease
- Dent disease type 1
- Dent disease type 2
- Denys-Drash syndrome
- DiGeorge syndrome
- EAST syndrome
- EEC syndrome
- EEC syndrome and related syndrome
- Ehlers-Danlos syndrome
- Ehlers-Danlos syndrome, musculocontractural type
- Ehlers-Danlos syndrome, musculocontractural type 1
