Disease browser and phenotype portal

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MSeqDR-LSDB
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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Hearing Loss Disease Portal

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Diarrhea (D003967)
Parent Node: Eye Diseases, Hereditary (D015785)
Parent Node: Intestinal Diseases (D007410)
Parent Node: Skin Abnormalities (D012868)
Parent Node: Vascular Diseases (D014652)
..Starting node ..Vascular Hyalinosis (C564750)
Child Nodes:
Sister Nodes:
..Aneurysm (D000783) 43
..Angiodysplasia (D016888) 2
..Angioedema (D000799) 5
..Angiomatosis (D000798) 10
..Aortic Diseases (D001018) 25
..Arterial Dissection with Lentiginosis (C563937)
..Arterial Occlusive Diseases (D001157) 39
..Arteriovenous Malformations (D001165) 12
..Arteritis (D001167) 7
..Calcification of Joints and Arteries (C565891)
..Capillary Leak Syndrome (D019559) 1
..CAROTID INTIMAL MEDIAL THICKNESS 2 (OMIM:608447)
..Cerebrovascular Disorders (D002561) 108
..Colitis, Ischemic (D017091)
..Compartment Syndromes (D003161) 3
..Coronary Artery Dissection, Spontaneous (C565153)
..Diabetic Angiopathies (D003925) 9
..Embolism and Thrombosis (D016769) 34
..Hand-Arm Vibration Syndrome (D053421)
..Hemorrhoids (D006484)
..Hemostatic Disorders (D020141) 48
..Hepatic Veno-Occlusive Disease (D006504) 1
..Hyperemia (D006940)
..Hypertension (D006973) 28
..Hypotension (D007022) 5
..Mesenteric Ischemia (D065666)
..Myocardial Ischemia (D017202) 28
..Optic Neuropathy, Ischemic (D018917) 1
..Pancytopenia and Occlusive Vascular Disease (C566836)
..Peripheral Vascular Diseases (D016491) 17
..Prehypertension (D058246)
..Pulmonary Veno-Occlusive Disease (D011668)
..Reperfusion Injury (D015427) 2
..Retinal Vein Occlusion (D012170)
..Scimitar Syndrome (D012587) 1
..Spinal Cord Vascular Diseases (D020758) 3
..Splenic Infarction (D013159)
..Superior Vena Cava Syndrome (D013479)
..Telangiectasis (D013684) 25
..Thoracic Outlet Syndrome (D013901) 2
..Varicocele (D014646)
..Varicose Veins (D014648) 2
..Vascular Fistula (D016157) 7
..Vascular Hyalinosis (C564750)
..Vascular Neoplasms (D019043)
..Vascular System Injuries (D057772)
..Vasculitis (D014657) 43
..Vasculopathy, Retinal, With Cerebral Leukodystrophy (C566007)
..Vasoplegia (D056987)
..Venous Insufficiency (D014689) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

11530

Name:

Vascular Hyalinosis

Definition:

Alternative IDs:

ParentIDs:

MESH:D003967|MESH:D007410|MESH:D012868|MESH:D014652|MESH:D015785

TreeNumbers:

C06.405.469/C564750 |C11.270/C564750 |C14.907/C564750 |C16.131.831/C564750 |C16.320.290/C564750 |C17.800.804/C564750 |C23.888.821.214/C564750

Synonyms:

Slim Mappings:

Reference:

MedGen: C564750
MeSH: C564750
OMIM: 277175;

Genes:

Phenotypes

1	HP:0000007	Autosomal recessive inheritance
2	HP:0002514	Cerebral calcification
3	HP:0007777	Chorioretinal scar
4	HP:0002573	Hematochezia
5	HP:0002024	Malabsorption
6	HP:0001029	Poikiloderma
7	HP:0002216	Premature graying of hair
8	HP:0002243	Protein-losing enteropathy
9	HP:0002138	Subarachnoid hemorrhage
10	HP:0002617	Vascular dilatation

Disease Causing ClinVar Variants