Experimental Factor Ontology
2169 terms(s) returned
| Term Type: | Record: 1151 to 1200 of 2169 Records | Page: 24 of 44, First Previous Next Last | Show Records Per Page |
- familial primary localized cutaneous amyloidosis
- familial primary pulmonary hypoplasia
- familial progressive hyper- and hypopigmentation
- familial progressive hyperpigmentation
- familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
- familial prostate carcinoma
- familial pseudohyperkalemia
- familial pterygium of the conjunctiva
- familial reactive perforating collagenosis
- familial recurrent peripheral facial palsy
- familial renal glucosuria
- familial restrictive cardiomyopathy
- familial retinal arterial macroaneurysm
- familial rhabdoid tumor
- familial scaphocephaly syndrome
- familial scaphocephaly syndrome, McGillivray type
- familial schizencephaly
- familial severe combined immunodeficiency
- familial sick sinus syndrome
- familial sleep-related hypermotor epilepsy
- familial spontaneous pneumothorax
- familial steroid-resistant nephrotic syndrome with sensorineural deafness
- familial syringomyelia
- familial temporal lobe epilepsy 2
- familial temporal lobe epilepsy 5
- familial temporal lobe epilepsy 7
- familial thoracic aortic aneurysm and aortic dissection
- familial thrombocytosis
- familial thrombomodulin anomalies
- familial thyroglossal duct cyst
- familial thyroid dyshormonogenesis
- familial tumoral calcinosis
- familial vesicoureteral reflux
- familial visceral amyloidosis
- familial visceral myopathy
- famililal cerebral cavernous malformations
- family based design
- family history
- family history of Alzheimer’s disease
- family history of breast cancer
- family history of cancer
- family history of diabetes
- family history of heart disease
- family history of high blood pressure
- family history of lung cancer
- family history of prostate cancer
- family history of upper gastrointestinal cancer
- family history of uterine fibroids
- family relationship
- family size
