Disease Index
9,486 diseasesinherited Creutzfeldt–Jakob disease
inherited digestive cancer-predisposing syndrome
human disease
inherited digestive tract tumor
human disease
inherited epidermolysis bullosa
Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues
Inherited giant platelet disorder
human disease
inherited gynecological tumor
human disease
inherited ichthyosis
instance of ichthyosis (disease) that is caused by an inherited modification of the individual's genome
inherited ichthyosis syndromic form
human disease
inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
inherited isolated nail anomaly
nail anomaly that is not part of a larger syndrome
inherited metabolic disorder
class of disease including endocrine diseases, nutritional diseases and metabolic diseases
ICD: E70MeSH: D008661
inherited nervous system cancer-predisposing syndrome
human disease
inherited neuroendocrine tumor
human disease
inherited non-syndromic ichthyosis
human disease
inherited prion disease
instance of prion disease that is caused by an inherited modification of the individual's genome
inherited pseudoxanthoma elasticum
Human disease
MeSH: D011561
inherited renal tubular disease
human disease
inherited renal tumor
human disease
inherited skin tumor
human disease
inherited soft tissue tumor
human disease
inherited syndrome with bone tumors as a major feature
human disease
inherited tumor
human disease
iniencephaly
rare form of neural tube defect in which a malformation of the cervico-occipital junction is associated with a malformation of the central nervous system
ICD: Q00.2
inosine triphosphatase deficiency
inherited condition caused by mutation in the ITPA gene
MeSH: C564127
insulin resistance
human disease
MeSH: D007333
Insulin-resistance syndrome type A
Insulin-resistance syndrome type B
insulinoma
tumor that produces too much insulin
ICD: C25.4MeSH: D007340
intellectual developmental disorder with autism and speech delay
human disease
intellectual disability
generalized neurodevelopmental disorder
ICD: F79MeSH: D008607