Experimental Factor Ontology
135 terms(s) returned
Term Type: | Record: 51 to 100 of 135 Records | Page: 2 of 3, First Previous Next Last | Show Records Per Page |
- Genetic malformation syndrome with odontal and/or periodontal component
- Genetic malformation syndrome with short stature
- Genetic mixed dermis disorder
- Genetic motor neuron disease
- Genetic multiple congenital anomalies/dysmorphic syndrome - variable intellectual disability
- Genetic muscular channelopathy
- Genetic neuro-ophthalmological disease
- Genetic neurodegenerative disease
- Genetic neurodegenerative disease with dementia
- Genetic neuromuscular disease
- Genetic neuromuscular junction disease
- Genetic neurovascular malformation
- Genetic non-syndromic central nervous system malformation
- Genetic non-syndromic renal or urinary tract malformation
- Genetic obesity
- Genetic overgrowth/obesity syndrome
- Genetic pancreatic disease
- Genetic periodic paralysis
- Genetic photodermatosis
- Genetic pigmentation anomaly of the skin
- Genetic polycythemia
- Genetic polyendocrinopathy
- Genetic porokeratosis
- Genetic posterior fossa malformation
- Genetic renal or urinary tract malformation
- Genetic renal tubular disease
- Genetic renal tumor
- Genetic respiratory malformation
- Genetic respiratory or mediastinal malformation
- Genetic skeletal muscle disease
- Genetic skin tumor
- Genetic skin vascular disorder
- Genetic soft tissue tumor
- Genetic subcutaneous tissue disorder
- Genetic susceptibility to infections due to particular pathogens
- Genetic syndrome with a Dandy-Walker malformation as major feature
- Genetic syndrome with a central nervous system malformation as major feature
- Genetic syndrome with a cerebellar malformation as major feature
- Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
- Genetic syndrome with limb malformations as a major feature
- Genetic syndrome with limb reduction defects
- Genetic syndromic esophageal malformation
- Genetic thrombotic microangiopathy
- Genetic tumor of hematopoietic and lymphoid tissues
- Genetic urogenital tract malformation
- Genetic urogenital tumor
- Genetic visceral malformation of the liver, biliary tract, pancreas or spleen
- Genetic vitreous-retinal disease
- Genodermatosis with ocular features
- Gerbode defect