Mondo Disease Ontology
1603 terms(s) returned
| Term Type: | Record: 751 to 800 of 1603 Records | Page: 16 of 33, First Previous Next Last | Show Records Per Page |
- familial melanoma
- familial meningioma
- familial mesial temporal lobe epilepsy
- familial mitral valve prolapse
- familial monosomy 7 syndrome
- familial mucolipidosis
- familial multiple discoid fibromas
- familial multiple fibrofolliculoma
- familial multiple lipomatosis
- familial multiple meningioma
- familial multiple nevi flammei
- familial multiple trichoepithelioma
- familial myelofibrosis
- familial nasal acilia
- familial nephrotic syndrome
- familial nonmedullary thyroid carcinoma
- familial omphalocele syndrome with facial dysmorphism
- familial or sporadic hemiplegic migraine
- familial ossifying fibroma
- familial osteodysplasia, Anderson type
- familial osteosclerosis
- familial ovarian cancer
- familial ovarian carcinoma
- familial pancreatic carcinoma
- familial panic disorder
- familial papillary or follicular thyroid carcinoma
- familial papillary thyroid carcinoma with renal papillary neoplasia
- familial parathyroid adenoma
- familial partial epilepsy
- familial partial lipodystrophy
- familial partial lipodystrophy, Dunnigan type
- familial partial lipodystrophy, Kobberling type
- familial partial paralysis
- familial periodic paralysis
- familial pityriasis rubra pilaris
- familial polycythemia
- familial porencephaly
- familial porphyria cutanea tarda
- 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
