Mondo Disease Ontology
2494 terms(s) returned
| Term Type: | Record: 1301 to 1350 of 2494 Records | Page: 27 of 50, First Previous Next Last | Show Records Per Page |
- hereditary inclusion-body myopathy
- hereditary intrinsic factor deficiency
- hereditary kidney oncocytoma
- hereditary leiomyomatosis and renal cell cancer
- hereditary lethal multiple congenital anomalies/dysmorphic syndrome
- hereditary lipodystrophy
- hereditary macular dystrophy
- hereditary methemoglobinemia
- hereditary mixed polyposis syndrome
- hereditary motor and sensory neuropathy
- hereditary motor and sensory neuropathy type 6
- hereditary motor and sensory neuropathy with acrodystrophy
- hereditary motor and sensory neuropathy, Okinawa type
- hereditary motor neuron disease
- hereditary mucoepithelial dysplasia
- hereditary mucosal leukokeratosis
- hereditary multiple osteochondromas
- 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
