Experimental Factor Ontology
11118 terms(s) returned
| Term Type: | Record: 5551 to 5600 of 11118 Records | Page: 112 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_eye morphology quality
- obsolete_eye movement quality
- obsolete_eye neoplasm
- obsolete_eye structure
- obsolete_eyelid border anomaly
- obsolete_eyelid disease
- obsolete_eyelid neoplasm
- obsolete_eyelid sagging measurement
- obsolete_eyelids malposition disorder
- obsolete_facial dermatosis
- obsolete_facial ganglion
- obsolete_facial hair thickness measurement
- obsolete_facial morphology quality
- obsolete_facial nerve disease
- obsolete_facial neuralgia
- obsolete_facial onset sensory and motor neuronopathy
- obsolete_facial pigmentation measurement
- obsolete_faciocardiorenal syndrome
- obsolete_facioscapulohumeral muscular dystrophy
- obsolete_factor VIII deficiency
- obsolete_factor type
- obsolete_factor type flag
- obsolete_fallopian tube disease
- obsolete_familial Dupuytren contracture
- obsolete_familial Mediterranean fever
- obsolete_familial abdominal aortic aneurysm
- obsolete_familial acute necrotizing encephalopathy
- obsolete_familial adenomatous polyposis due to 5q22.2 microdeletion
- obsolete_familial adrenal hypoplasia with absent pituitary luteinizing hormone
- obsolete_familial amyloid neuropathy
- obsolete_familial amyotrophic lateral sclerosis
- obsolete_familial anetoderma
- obsolete_familial angiolipomatosis
- obsolete_familial apolipoprotein C-II deficiency
- obsolete_familial atrial fibrillation
- obsolete_familial atrial myxoma
- obsolete_familial atypical multiple mole melanoma syndrome
- obsolete_familial avascular necrosis of femoral head
- obsolete_familial benign copper deficiency
- obsolete_familial benign flecked retina
- obsolete_familial bicuspid aortic valve
- obsolete_familial cardiomyopathy
- obsolete_familial caudal dysgenesis
- obsolete_familial clubfoot due to 17q23.1q23.2 microduplication
- obsolete_familial clubfoot due to 5q31 microdeletion
- obsolete_familial clubfoot due to PITX1 point mutation
- obsolete_familial clubfoot with or without associated lower limb anomalies
- obsolete_familial combined hyperlipidemia
- obsolete_familial congenital mirror movements
- obsolete_familial congenital palsy of trochlear nerve
