Kidney Tissue Atlas Ontology
78 terms(s) returned
| Term Type: | Record: 1 to 50 of 78 Records | Page: 1 of 2, First Previous Next Last | Show Records Per Page |
- Galloway-Mowat syndrome
- Galloway-Mowat syndrome 1
- Galloway-Mowat syndrome 2, X-linked
- Galloway-Mowat syndrome 3
- Galloway-Mowat syndrome 4
- Galloway-Mowat syndrome 5
- Galloway-Mowat syndrome 6
- Galloway-Mowat syndrome 7
- Galloway-Mowat syndrome 8
- Gitelman syndrome
- Graham-Boyle-Troxell syndrome
- galactokinase deficiency
- galactose epimerase deficiency
- galactosemia
- galactosemia 4
- gastroenteritis
- gastrointestinal mucositis
- general tumor grading characteristic
- generalized galactose epimerase deficiency
- genetic biliary tract disease
- genetic cardiac anomaly
- genetic central nervous system and retinal vascular disease
- genetic cerebral small vessel disease
- genetic dementia
- genetic endocrine growth disease
- genetic epidermal appendage anomaly
- genetic head and neck malformation
- genetic hyperparathyroidism
- genetic hypertension
- genetic hypoparathyroidism
- genetic infertility
- genetic lethal multiple congenital anomalies/dysmorphic syndrome
- genetic macular dystrophy
- genetic multiple congenital anomalies/dysmorphic syndrome
- genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability
- genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
- genetic nail anomaly
- genetic nervous system disorder
- genetic otorhinolaryngologic disease
- genetic otorhinolaryngological malformation
- genetic parenchymatous liver disease
- genetic peripheral neuropathy
- genetic sebaceous gland anomaly
- genetic skin disease
- genetic syndromic Pierre Robin syndrome
- genetic systemic or rheumatologic disease
- genetic vascular anomaly
- genetic vascular tumor
- genetic vs non-genetic etiology
- genodermatosis with ocular features
