Mondo Disease Ontology
2673 terms(s) returned
| Term Type: | Record: 1401 to 1450 of 2673 Records | Page: 29 of 54, First Previous Next Last | Show Records Per Page |
- hereditary multiple osteochondromas
- hereditary myelopathy, dog
- hereditary myopathy with lactic acidosis due to ISCU deficiency
- hereditary narcolepsy
- hereditary neoplastic syndrome
- hereditary nephritis
- hereditary neuro-ophthalmological disease
- hereditary neurocutaneous angioma
- hereditary neuroendocrine tumor of small intestine
- hereditary neurological disease
- hereditary neurological disease, non-human animal
- hereditary neuromuscular disease
- hereditary neuropathy with liability to pressure palsies
- hereditary neutrophilia
- hereditary nonpolyposis colon cancer
- hereditary nonpolyposis colorectal cancer, MSH6-related, rhesus monkey
- hereditary optic atrophy
- hereditary optic neuropathy
- hereditary otorhinolaryngologic disease
- hereditary painful callosities
- hereditary palmoplantar keratoderma
- hereditary palmoplantar keratoderma, Gamborg-Nielsen type
- hereditary pancreatitis, dog
- hereditary pancreatitis, non-human animal
- hereditary papillary renal cell carcinoma
- hereditary papulotranslucent acrokeratoderma
- hereditary periodic fever syndrome
- hereditary peripheral neuropathy
- hereditary persistence of fetal hemoglobin
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- hereditary persistence of fetal hemoglobin-intellectual disability syndrome
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hereditary pheochromocytoma-paraganglioma
- hereditary photodermatosis
- hereditary poikiloderma
- hereditary progressive chorea without dementia
- hereditary progressive mucinous histiocytosis
- hereditary pulmonary alveolar proteinosis
- hereditary recurrent myoglobinuria
- hereditary renal cell carcinoma
- hereditary renal hypouricemia
- hereditary retinoblastoma
- hereditary sclerosing poikiloderma with tendon and pulmonary involvement
- hereditary sclerosing poikiloderma, Weary type
- hereditary sebaceous gland anomaly
- hereditary sensorimotor neuropathy with hyperelastic skin
- hereditary sensory and autonomic neuropathy
- hereditary sensory and autonomic neuropathy type 1
- hereditary sensory and autonomic neuropathy type 2
- hereditary sensory and autonomic neuropathy type 4
