Experimental Factor Ontology
94656 terms(s) returned
| Term Type: | Record: 8651 to 8700 of 94656 Records | Page: 174 of 1894, First Previous Next Last | Show Records Per Page |
- Colombian in Medellin, Colombia (1KGP)
- Colonic diverticula
- Color vision defect
- Color-vision disease
- Colorado tick fever
- Coloured
- Columba livia
- Columbia ecotype
- Coma
- Combined T and B cell immunodeficiency
- Combined hyperlipidemia
- Combined immunodeficiency
- Combined immunodeficiency T+ B+ due to partial RAG1 deficiency
- Combined immunodeficiency with facio-oculo-skeletal anomalies
- Combined oxidative phosphorylation defect type 21
- Combined oxidative phosphorylation defect type 23
- Combined oxidative phosphorylation defect type 24
- Combined oxidative phosphorylation defect type 26
- Combined oxidative phosphorylation defect type 27
- Combined oxidative phosphorylation defect type 30
- Combined pituitary hormone deficiencies, genetic forms
- Comma-D
- Common Hematopoietic Neoplasm
- Common atrium
- Commotio Cordis
- Comoros
- Complete duplication of proximal phalanx of the thumb
- Complete duplication of thumb phalanx
- Complete right bundle branch block
- Complex Cyst of Kidney
- Complex chromosomal rearrangement
- Complex febrile seizure
- Compton-North congenital myopathy
- Compulsive behaviors
- Concave nasal ridge
- Concentric hypertrophic cardiomyopathy
- Concomitant strabismus
- Conductive deafness - ptosis - skeletal anomalies
- Conductive hearing impairment
- Cone dystrophy
- Cone rod dystrophy
- Confusion
- Congenital absence of the eyebrow/eyelashes
- Congenital absence of upper arm and forearm with hand present, bilateral
- Congenital absence of upper arm and forearm with hand present, unilateral
- Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency
- Congenital agranulocytosis
- Congenital alpha2 antiplasmin deficiency
- Congenital alveolar capillary dysplasia
- Congenital and infantile nephrotic syndrome
