Mondo Disease Ontology
1492 terms(s) returned
| Term Type: | Record: 551 to 600 of 1492 Records | Page: 12 of 30, First Previous Next Last | Show Records Per Page |
- Gout
- Graham Little-Piccardi-Lassueur syndrome
- Graham-Boyle-Troxell syndrome
- Grant syndrome
- Granulocytic hyperplasia
- Granulocytic hypoplasia
- Granulovacuolar degeneration
- Graves disease
- Graves disease, susceptibility to, 1
- Graves disease, susceptibility to, 2
- Graves disease, susceptibility to, X-linked 1
- Graves disease, susceptibility to, X-linked 2
- Gray matter heterotopia
- Grayson-Wilbrandt corneal dystrophy
- Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome
- Greig cephalopolysyndactyly-contiguous gene syndrome
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Grisel syndrome
- Growth abnormality
- Growth delay
- Grubben-de Cock-Borghgraef syndrome
- Guillain-Barr-like polyradiculoneuropathy, dog
- Guillain-Barr-like polyradiculoneuropathy, domestic cat
- Guillain-Barr-like polyradiculoneuropathy, non-human animal
- Guillain-Barre syndrome
- Guillain-Barre syndrome, familial
- Guillouet-Gordon syndrome
- Gunneridae
- Guttmacher syndrome
- Gynecomastia
- gait apraxia
- galactokinase deficiency
- galactolipid
- galactorrhea
- galactorrhoea-hyperprolactinaemia
- galactose epimerase deficiency
- galactose metabolic process
- galactose-6-sulfurylase activity
- galactosemia
- galactosemia 4
- galactosemia, kangaroo
- galactosemia, non-human animal
- galactosialidosis
- galactosialidosis, dog
- galactosialidosis, non-human animal
- galactosidase activity
