Kidney Tissue Atlas Ontology
98 terms(s) returned
| Term Type: | Record: 1 to 50 of 98 Records | Page: 1 of 2, First Previous Next Last | Show Records Per Page |
- Fabry disease
- Fanconi anemia
- Fanconi anemia complementation group A
- Fanconi anemia complementation group C
- Fanconi anemia complementation group D1
- Fanconi anemia complementation group D2
- Fanconi anemia complementation group E
- Fanconi anemia complementation group G
- Fanconi anemia complementation group I
- Fanconi anemia complementation group L
- Fanconi anemia complementation group N
- Fanconi anemia complementation group O
- Fanconi anemia complementation group P
- Fanconi anemia complementation group Q
- Fanconi anemia complementation group T
- Fanconi anemia complementation group U
- Fanconi anemia complementation group V
- Fanconi anemia complementation group b
- Fanconi anemia complementation group f
- Fanconi anemia complementation group j
- Fanconi anemia complementation group r
- Fanconi anemia, complementation group S
- Fanconi anemia, complementation group W
- Fanconi renotubular syndrome
- Fanconi renotubular syndrome 1
- Fanconi renotubular syndrome 2
- Fanconi renotubular syndrome 3
- Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young
- Fanconi renotubular syndrome 5
- Fibulo-ulnar hypoplasia-renal anomalies syndrome
- Franceschini Vardeu Guala syndrome
- Fraser syndrome
- Fraser syndrome 1
- Fraser syndrome 2
- Fraser syndrome 3
- Frasier syndrome
- face disease
- facial cleft
- faciocardiorenal syndrome
- familial Mediterranean fever
- familial Mediterranean fever, autosomal dominant
- familial cardiomyopathy
- familial cystic renal disease
- familial dilated cardiomyopathy
- familial gestational hyperthyroidism
- familial hemolytic anemia
- familial hyperaldosteronism
- familial hyperthyroidism due to mutations in TSH receptor
- familial hypertrophic cardiomyopathy
- familial idiopathic steroid-resistant nephrotic syndrome
