Mondo Disease Ontology
1872 terms(s) returned
| Term Type: | Record: 851 to 900 of 1872 Records | Page: 18 of 38, First Previous Next Last | Show Records Per Page |
- familial primary hyperparathyroidism
- familial primary hypomagnesemia
- familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- familial primary hypomagnesemia with hypocalcuria
- familial primary hypomagnesemia with normocalciuria and normocalcemia
- familial primary hypomagnesemia with normocalcuria
- 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 supernumerary nipples
- familial syringomyelia
- familial temporal lobe epilepsy 2
- familial temporal lobe epilepsy 3
- familial temporal lobe epilepsy 4
- familial temporal lobe epilepsy 5
- familial temporal lobe epilepsy 6
- familial temporal lobe epilepsy 7
- familial temporal lobe epilepsy 8
- familial thoracic aortic aneurysm and aortic dissection
- familial thoracic aortic aneurysm, dog
- familial thoracic aortic aneurysm, non-human animal
- 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
- fanconi anemia, complementation group 10
