Disease Index
9,486 diseaseshereditary neurocutaneous malformation
MeSH: C536364
hereditary neuroendocrine tumor of small intestine
instance of neuroendocrine tumor of the small intestine that is caused by an inherited modification of the individual's genome
hereditary neuropathy with liability to pressure palsies
peripheral neuropathy
MeSH: C536965
hereditary neutrophilia
human disease
MeSH: C563010
hereditary optic neuropathy
human disease
hereditary palmoplantar keratoderma
instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome
hereditary palmoplantar keratoderma, Gamborg-Nielsen type
hereditary pancreatitis
congenital disorder of digestive system
hereditary pediatric Behçet-like disease
human disease
hereditary periodic fever syndrome
instance of periodic fever syndrome that is caused by an inherited modification of the individual's genome
hereditary persistence of alpha-fetoprotein
Hereditary persistence of alpha-fetoprotein is a benign genetic condition characterized by persistence of high alpha-fetoprotein (AFP) levels throughout life, with no associated clinical disability and thus no need for specific therapy
hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
Hereditary persistence of fetal hemoglobin (HPFH) associated with beta-thalassemia (see this term) is characterized by high hemoglobin (Hb) F levels and an increased number of fetal-Hb-containing-cells
hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
human disease
hereditary pheochromocytoma-paraganglioma
hereditary poikiloderma
human disease
Hereditary progressive mucinous histiocytosis
human disease
MeSH: C564186
hereditary proximal myopathy with early respiratory failure
human disease
MeSH: C566343
hereditary pyropoikilocytosis
autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency
MeSH: C563004
hereditary renal cell carcinoma
human disease
MeSH: C536851
hereditary renal hypouricemia
MeSH: C537757
Hereditary resistance to anti-vitamin K
Hereditary sclerosing poikiloderma
human disease
ICD: Q82.8MeSH: C562824
hereditary sclerosing poikiloderma with tendon and pulmonary involvement
human disease
hereditary sensorimotor neuropathy with hyperelastic skin
human disease
hereditary sensory and autonomic neuropathy
congenital disorder of nervous system
MeSH: D009477
hereditary sensory and autonomic neuropathy type 1
hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance
hereditary sensory and autonomic neuropathy type 2
hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood
hereditary sensory and autonomic neuropathy type 2A
hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has material basis in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13
hereditary sensory and autonomic neuropathy type 5
hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has material basis in homozygous mutation in the NGF gene on chromosome 1p13
Hereditary sensory and autonomic neuropathy type 6
genetic disporder