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Disease	Synonyms	Description
intermittent asthma		A chronic asthma that is characterized by severity..[+] A chronic asthma that is characterized by severity with symptoms two or fewer days per week, nighttime awakenings two or fewer times per month, use of short-acting beta agonist for symptom control two or fewer days per week and no interference with normal activity. [-]
intracranial meningioma		A meningioma that arises within the cranial cavity..[+] A meningioma that arises within the cranial cavity. [-]
IgA pemphigus		A pemphigus that is characterized by painful and p..[+] A pemphigus that is characterized by painful and pruritic vesiculopustular eruptions. These eruptions form as a result of circulating IgA antibodies against keratinocyte cell surface components responsible for cell to cell adherence. [-]
IDH-mutant anaplastic astrocytoma		An anaplastic astrocytoma carrying IDH mutations.
IDH-wildtype anaplastic astrocytoma		An anaplastic astrocytoma lacking mutations in IDH..[+] An anaplastic astrocytoma lacking mutations in IDH1 or IDH2 genes. [-]
IDH-wildtype glioblastoma		A glioblastoma that is characterized by high cellu..[+] A glioblastoma that is characterized by high cellularity, high mitotic activity, necrosis or microvascular proliferation and that lacks mutations in IDH genes. [-]
IDH-mutant and 1p/19q-codeleted oligodendroglioma	anaplastic oligodendroglioma, IDH-mutant and 1p/19.. [+] anaplastic oligodendroglioma, IDH-mutant and 1p/19q-codeleted; Oligodendroglioma, IDH-mutant and 1p/19q-codeleted [-]	An anaplastic oligodendroglioma that has_material_..[+] An anaplastic oligodendroglioma that has_material_basis_in IDH gene family mutation and combined whole-arm losses of 1p and 19q (1p/19q codeletion). [-]
immunoglobulin light chain amyloidosis	AL amyloidosis; Light chain amyloidosis; Amyloidos.. [+] AL amyloidosis; Light chain amyloidosis; Amyloidosis primary systemic; Primary AL amyloidosis; Primary systemic AL amyloidosis; Primary systemic amyloidosis; Systemic AL amyloidsis [-]	An amyloidosis that is characterized by misfolded ..[+] An amyloidosis that is characterized by misfolded and aggregated amyloidogenic immunoglobulin light chains produced by marrow clonal plasma cells. [-]
immunoglobulin heavy chain amyloidosis	Ig heavy-chain–associated amyloidosis; AH amyloido.. [+] Ig heavy-chain–associated amyloidosis; AH amyloidosis; Amyloidosis derived from immunoglobulin heavy chain; Heavy chain amyloidosis [-]	An amyloidosis that is characterized by the aggreg..[+] An amyloidosis that is characterized by the aggregation and deposition of amyloid fibrils composed of monoclonal immunoglobulin heavy-chain fragments, usually produced by a plasma cell neoplasm. [-]
immunoglobulin heavy-and-light chain	Ig heavy-and-light-chain amyloidosis; AH/AL amyloi.. [+] Ig heavy-and-light-chain amyloidosis; AH/AL amyloidosis [-]	An amyloidosis that is characterized by both Ig he..[+] An amyloidosis that is characterized by both Ig heavy chains and LC contribute to the amyloid fibrils. [-]
intracranial berry aneurysm 1		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 7q11.2. [-]
intracranial berry aneurysm 3		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 1p36. [-]
intracranial berry aneurysm 5		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome Xp22. [-]
intracranial berry aneurysm 6		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 9p21. [-]
intracranial berry aneurysm 7		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 11q24-q25. [-]
intracranial berry aneurysm 9		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 2q33.1. [-]
intracranial berry aneurysm 10		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and has been mapped to chromosome 8q12.1. [-]
intracranial berry aneurysm 12		An intracranial berry aneurysm that is characteriz..[+] An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and that has_material_basis_in heterozygous mutation in the THSD1 gene on chromosome 13q14. [-]
intellectual developmental disorder with cardiac arrhythmia	GNB5-related intellectual disability-cardiac arrhy.. [+] GNB5-related intellectual disability-cardiac arrhythmia syndrome [-]	A syndrome that is characterized by delayed psycho..[+] A syndrome that is characterized by delayed psychomotor development, severe intellectual disability with poor or absent speech, and bradycardia and/or cardiac sinus arrhythmias and that has_material_basis_in homozygous or compound heterozygous mutation in the GNB5 gene on chromosome 15q21. [-]
inclusion body myopathy and brain white matter abnormalities	multisystem proteinopathy 6	An inclusion body myopathy with Paget disease of b..[+] An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that is characterized by proximal limb girdle muscle weakness affecting the lower and upper limbs and resulting in gait difficulties and scapular winging and that has_material_basis_in heterozygous mutation in the ANXA11 gene on chromosome 10q22. [-]

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