Experimental Factor Ontology
11118 terms(s) returned
| Term Type: | Record: 5651 to 5700 of 11118 Records | Page: 114 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_familial keratoacanthoma
- obsolete_familial lambdoid synostosis
- obsolete_familial lipoprotein lipase deficiency
- obsolete_familial long QT syndrome
- obsolete_familial median cleft of the upper and lower lips
- obsolete_familial medullary thyroid carcinoma
- obsolete_familial melanoma
- obsolete_familial mesial temporal lobe epilepsy with febrile seizures
- obsolete_familial multiple fibrofolliculoma
- obsolete_familial multiple lipomatosis
- obsolete_familial multiple nevi flammei
- obsolete_familial multiple trichoepithelioma
- obsolete_familial nonmedullary thyroid carcinoma
- obsolete_familial omphalocele syndrome with facial dysmorphism
- obsolete_familial or sporadic hemiplegic migraine
- obsolete_familial osteodysplasia, Anderson type
- obsolete_familial ovarian cancer
- obsolete_familial pancreatic carcinoma
- obsolete_familial papillary or follicular thyroid carcinoma
- obsolete_familial papillary thyroid carcinoma with renal papillary neoplasia
- obsolete_familial parathyroid adenoma
- obsolete_familial partial epilepsy
- obsolete_familial partial lipodystrophy
- obsolete_familial partial lipodystrophy, Dunnigan type
- obsolete_familial porencephaly
- obsolete_familial primary hyperparathyroidism
- obsolete_familial primary hypomagnesemia
- obsolete_familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- obsolete_familial primary hypomagnesemia with hypocalcuria
- obsolete_familial primary hypomagnesemia with normocalciuria and normocalcemia
- obsolete_familial primary hypomagnesemia with normocalcuria
- obsolete_familial primary localized cutaneous amyloidosis
- obsolete_familial primary pulmonary hypoplasia
- obsolete_familial progressive hyper- and hypopigmentation
- obsolete_familial progressive hyperpigmentation
- obsolete_familial pseudohyperkalemia
- obsolete_familial reactive perforating collagenosis
- obsolete_familial recurrent peripheral facial palsy
- obsolete_familial restrictive cardiomyopathy
- obsolete_familial retinal arterial macroaneurysm
- obsolete_familial rhabdoid tumor
- obsolete_familial scaphocephaly syndrome
- obsolete_familial scaphocephaly syndrome, McGillivray type
- obsolete_familial sick sinus syndrome
- obsolete_familial spontaneous pneumothorax
- obsolete_familial steroid-resistant nephrotic syndrome with sensorineural deafness
- obsolete_familial syringomyelia
- obsolete_familial thoracic aortic aneurysm and aortic dissection
- obsolete_familial thrombocytosis
- obsolete_familial thrombomodulin anomalies
