Experimental Factor Ontology
11043 terms(s) returned
| Term Type: | Record: 701 to 750 of 11043 Records | Page: 15 of 221, First Previous Next Last | Show Records Per Page |
- obsolete eyelids malposition disorder
- obsolete facial hypertrichosis
- obsolete facial nerve palsy due to herpes zoster infection
- obsolete familial cerebral cavernous malformation
- obsolete familial dyskinesia and facial myokymia
- obsolete familial hypercholanemia
- obsolete familial hyperreninemic hypoaldosteronism type 1
- obsolete familial infantile gigantism
- obsolete familial isolated dilated cardiomyopathy
- obsolete familial isolated restrictive cardiomyopathy
- obsolete familial lambdoid synostosis
- obsolete familial mesial temporal lobe epilepsy with febrile seizures
- obsolete familial patent arterial duct
- obsolete familial pityriasis rubra pilaris
- obsolete fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
- obsolete female infertility due to an anomaly of ovarian function of genetic origin
- obsolete fetal anticonvulsant syndrome
- obsolete fibrous dysplasia of bone
- obsolete food allergy
- obsolete gastroduodenal malformation
- obsolete gastroesophageal disease
- obsolete generalized bulbospinal muscular atrophy
- obsolete generalized isolated dystonia
- obsolete generalized pustular psoriasis
- obsolete genetic cardiac rhythm disease
- obsolete genetic central nervous system and retinal vascular disease
- obsolete genetic hair anomaly
- obsolete genetic hypertension
- obsolete genetic infertility
- obsolete genetic multiple congenital anomalies/dysmorphic syndrome
- obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability
- obsolete genetic nail anomaly
- obsolete genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
- obsolete genetic transient congenital hypothyroidism
- obsolete global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome
- obsolete glucose transmembrane transporter activity
- obsolete glycogen storage disease VIII
- obsolete glycosyl compound metabolic process
- obsolete glycosylation
- obsolete goniodysgenesis
- obsolete gonosome number anomaly
- obsolete gonosome structural anomaly
- obsolete guard cell
- obsolete hair defect-photosensitivity-intellectual disability syndrome
- obsolete head visceral muscle primordium
- obsolete hemifacial microsomia
- obsolete hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
- obsolete hemorrhagic disorder due to a constitutional platelet anomaly
- obsolete hereditary ATTR amyloidosis
- obsolete hereditary angioedema with normal C1Inh
