1. Gene
  2. TSC2 - TSC complex subunit 2 Gene

TSC2 - TSC complex subunit 2 Gene

中文名称:TSC 复杂亚基 2

种属: Homo sapiens

同用名: LAM; TSC4; PPP1R160

基因 ID: 7249 | 基因类型: protein coding

关于 TSC2

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:2,047,985-2,089,491 (from NCBI)

This gene has 69 transcripts (splice variants), 204 orthologues, 2 paralogues and is associated with 165 phenotypes. Ubiquitous expression in testis (RPKM 18.9), thyroid (RPKM 12.5) and 25 other tissues.

功能概要

该基因是一种肿瘤抑制基因,编码生长抑制蛋白 tuberin。 Tuberin 与 hamartin 相互作用形成 TSC 蛋白复合物,该复合物在细胞生长的控制中发挥作用。这种 TSC 蛋白复合物负向调节哺乳动物雷帕霉素靶蛋白复合物 1 (mTORC1) 信号,后者是合成代谢细胞生长的主要调节因子。该基因的突变与结节性硬化症和淋巴管平滑肌瘤病有关。[RefSeq 提供,2022 年 5 月]

This gene is a tumor suppressor gene that encodes the growth inhibitory protein tuberin. Tuberin interacts with hamartin to form the TSC protein complex which functions in the control of cell growth. This TSC protein complex negatively regulates mammalian target of rapamycin complex 1 (mTORC1) signaling which is a major regulator of anabolic cell growth. Mutations in this gene have been associated with tuberous sclerosis and lymphangioleiomyomatosis. [provided by RefSeq, May 2022]

TSC2 基因产物(86)

mRNA Protein Name
NM_000548.5 NP_000539.2 tuberin isoform 1
NM_001077183.3 NP_001070651.1 tuberin isoform 4
NM_001114382.3 NP_001107854.1 tuberin isoform 5
NM_001318827.2 NP_001305756.1 tuberin isoform 6
NM_001318829.2 NP_001305758.1 tuberin isoform 7
NM_001318831.2 NP_001305760.1 tuberin isoform 8
NM_001318832.2 NP_001305761.1 tuberin isoform 9
NM_001363528.2 NP_001350457.1 tuberin isoform 10
NM_001370404.1 NP_001357333.1 tuberin isoform 11
NM_001370405.1 NP_001357334.1 tuberin isoform 12
NM_001406663.1 NP_001393592.1 tuberin isoform 13
NM_001406664.1 NP_001393593.1 tuberin isoform 14
NM_001406665.1 NP_001393594.1 tuberin isoform 15
NM_001406667.1 NP_001393596.1 tuberin isoform 16
NM_001406668.1 NP_001393597.1 tuberin isoform 17
NM_001406670.1 NP_001393599.1 tuberin isoform 18
NM_001406671.1 NP_001393600.1 tuberin isoform 19
NM_001406673.1 NP_001393602.1 tuberin isoform 20
NM_001406675.1 NP_001393604.1 tuberin isoform 21
NM_001406676.1 NP_001393605.1 tuberin isoform 22
NM_001406677.1 NP_001393606.1 tuberin isoform 23
NM_001406678.1 NP_001393607.1 tuberin isoform 24
NM_001406679.1 NP_001393608.1 tuberin isoform 25
NM_001406680.1 NP_001393609.1 tuberin isoform 26
NM_001406681.1 NP_001393610.1 tuberin isoform 27
NM_001406682.1 NP_001393611.1 tuberin isoform 28
NM_001406683.1 NP_001393612.1 tuberin isoform 28
NM_001406684.1 NP_001393613.1 tuberin isoform 29
NM_001406685.1 NP_001393614.1 tuberin isoform 30
NM_001406686.1 NP_001393615.1 tuberin isoform 30
NM_001406687.1 NP_001393616.1 tuberin isoform 31
NM_001406688.1 NP_001393617.1 tuberin isoform 31
NM_001406689.1 NP_001393618.1 tuberin isoform 32
NM_001406690.1 NP_001393619.1 tuberin isoform 33
NM_001406691.1 NP_001393620.1 tuberin isoform 34
NM_001406692.1 NP_001393621.1 tuberin isoform 35
NM_001406693.1 NP_001393622.1 tuberin isoform 35
NM_001406694.1 NP_001393623.1 tuberin isoform 35
NM_001406695.1 NP_001393624.1 tuberin isoform 36
NM_001406696.1 NP_001393625.1 tuberin isoform 36
NM_001406697.1 NP_001393626.1 tuberin isoform 36
NM_001406698.1 NP_001393627.1 tuberin isoform 37
NM_021055.3 NP_066399.2 tuberin isoform 2
NM_000548.5 NP_000539.2 tuberin isoform 1
NM_001077183.3 NP_001070651.1 tuberin isoform 4
NM_001114382.3 NP_001107854.1 tuberin isoform 5
NM_001318827.2 NP_001305756.1 tuberin isoform 6
NM_001318829.2 NP_001305758.1 tuberin isoform 7
NM_001318831.2 NP_001305760.1 tuberin isoform 8
NM_001318832.2 NP_001305761.1 tuberin isoform 9
NM_001363528.2 NP_001350457.1 tuberin isoform 10
NM_001370404.1 NP_001357333.1 tuberin isoform 11
NM_001370405.1 NP_001357334.1 tuberin isoform 12
NM_001406663.1 NP_001393592.1 tuberin isoform 13
NM_001406664.1 NP_001393593.1 tuberin isoform 14
NM_001406665.1 NP_001393594.1 tuberin isoform 15
NM_001406667.1 NP_001393596.1 tuberin isoform 16
NM_001406668.1 NP_001393597.1 tuberin isoform 17
NM_001406670.1 NP_001393599.1 tuberin isoform 18
NM_001406671.1 NP_001393600.1 tuberin isoform 19
NM_001406673.1 NP_001393602.1 tuberin isoform 20
NM_001406675.1 NP_001393604.1 tuberin isoform 21
NM_001406676.1 NP_001393605.1 tuberin isoform 22
NM_001406677.1 NP_001393606.1 tuberin isoform 23
NM_001406678.1 NP_001393607.1 tuberin isoform 24
NM_001406679.1 NP_001393608.1 tuberin isoform 25
NM_001406680.1 NP_001393609.1 tuberin isoform 26
NM_001406681.1 NP_001393610.1 tuberin isoform 27
NM_001406682.1 NP_001393611.1 tuberin isoform 28
NM_001406683.1 NP_001393612.1 tuberin isoform 28
NM_001406684.1 NP_001393613.1 tuberin isoform 29
NM_001406685.1 NP_001393614.1 tuberin isoform 30
NM_001406686.1 NP_001393615.1 tuberin isoform 30
NM_001406687.1 NP_001393616.1 tuberin isoform 31
NM_001406688.1 NP_001393617.1 tuberin isoform 31
NM_001406689.1 NP_001393618.1 tuberin isoform 32
NM_001406690.1 NP_001393619.1 tuberin isoform 33
NM_001406691.1 NP_001393620.1 tuberin isoform 34
NM_001406692.1 NP_001393621.1 tuberin isoform 35
NM_001406693.1 NP_001393622.1 tuberin isoform 35
NM_001406694.1 NP_001393623.1 tuberin isoform 35
NM_001406695.1 NP_001393624.1 tuberin isoform 36
NM_001406696.1 NP_001393625.1 tuberin isoform 36
NM_001406697.1 NP_001393626.1 tuberin isoform 36
NM_001406698.1 NP_001393627.1 tuberin isoform 37
NM_021055.3 NP_066399.2 tuberin isoform 2
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables GTPase activator activity IDA
IDA: 通过直接分析推断
9045618 GOA
enables Hsp90 protein binding IPI
IPI: 通过物理相互作用推断
29127155 GOA
enables phosphatase binding IDA
IDA: 通过直接分析推断
19389623 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
9580671 GOA
enables protein homodimerization activity IPI
IPI: 通过物理相互作用推断
10585443 GOA
enables small GTPase binding IPI
IPI: 通过物理相互作用推断
25936802 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in anoikis IGI
IGI: 通过遗传相互作用推断
23778976 GOA
involved in cellular response to starvation IDA
IDA: 通过直接分析推断
24529379 GOA
involved in negative regulation of TOR signaling IDA
IDA: 通过直接分析推断
22795129 GOA
involved in negative regulation of TOR signaling IGI
IGI: 通过遗传相互作用推断
23778976 GOA
involved in negative regulation of TORC1 signaling IDA
IDA: 通过直接分析推断
9045618 GOA
involved in positive regulation of macroautophagy IGI
IGI: 通过遗传相互作用推断
23778976 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
NOT located in Golgi apparatus IDA
IDA: 通过直接分析推断
10585443 GOA
located in Golgi apparatus IDA
IDA: 通过直接分析推断
8806680 GOA
part of TSC1-TSC2 complex IDA
IDA: 通过直接分析推断
9580671 GOA
part of TSC1-TSC2 complex IPI
IPI: 通过物理相互作用推断
22795129 GOA
colocalizes with cytoplasm IDA
IDA: 通过直接分析推断
17114346 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
9580671 GOA
located in cytosol IDA
IDA: 通过直接分析推断
10585443 GOA
is active in lysosomal membrane IDA
IDA: 通过直接分析推断
24529379 GOA
located in lysosome IDA
IDA: 通过直接分析推断
25936802 GOA
located in membrane IDA
IDA: 通过直接分析推断
16636147 GOA
NOT located in nucleus IDA
IDA: 通过直接分析推断
16636147 GOA
located in nucleus IDA
IDA: 通过直接分析推断
17114346 GOA
located in perinuclear region of cytoplasm IDA
IDA: 通过直接分析推断
8806680 GOA
is active in postsynaptic density EXP
EXP: 通过实验结果推断
27898073 GOA
is active in postsynaptic density IDA
IDA: 通过直接分析推断
27898073 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

TSC2 蛋白结构

DUF3384

DUF3384: Domain of unknown function (DUF3384) (53 - 469)

Tuberin

Tuberin: Tuberin (555 - 904)

Rap_GAP

Rap_GAP: Rap/ran-GAP (1561 - 1740)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1807 a.a.
蛋白主名 其他名称

tuberin

protein phosphatase 1, regulatory subunit 160

TSC2 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
TSC2 P49815 SGK1 Homo sapiens O00141
Anti Tag CoIP
27451907
种属内
TSC2 P49815 SGK1 Homo sapiens O00141
FRET
27451907
种属内
TSC2 P49815 SGK1 Homo sapiens O00141
Anti Bait CoIP
27451907
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Y2H
9580671
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Anti Tag CoIP
25263562
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Anti Tag CoIP
33436626
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Anti Bait CoIP
21134130
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Anti Bait CoIP
20412061
种属内
TSC2 P49815 TSC1 Homo sapiens Q92574
Anti Bait CoIP
17693255
种属内
TSC2 P49815 SIRT1 Homo sapiens Q96EB6
Anti Bait CoIP
20169165
种属内
TSC2 P49815 YWHAZ Homo sapiens P63104
Far-WB
15161933
种属内
TSC2 P49815 YWHAZ Homo sapiens P63104
Pull Down
15161933
种属内
TSC2 P49815 YWHAZ Homo sapiens P63104
Filter Binding
12438239
种属内
TSC2 P49815 YWHAZ Homo sapiens P63104
Pull Down
12176984
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
Experimental Interac
12468542
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
CoIP
12582162
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
Y2H
12468542
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
CoIP
12468542
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
CoIP
15324660
种属内
TSC2 P49815 YWHAB Homo sapiens P31946
Pull Down
20169078
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Lymphangioleiomyomatosis

Lymphangiomyomatosis

LAM

Lung Lymphangioleiomyomatosis

Pulmonary Lymphangioleiomyomatosis

Lymphangioleiomyomatosis, Somatic

Lymphangio-Myomatosis

Focal Cortical Dysplasia, Type Ii

Focal Cortical Dysplasia Of Taylor

Cortical Dysplasia Of Taylor

Cdt

Fcdt

Isolated Focal Cortical Dysplasia Type Ii

FCORD2

Fcd2

Focal Cortical Dysplasia Type 2

Cortical Dysplasia Of Taylor, Dysplasia Only

Focal Cortical Dysplasia, Type Ii, Somatic

Focal Cortical Dysplasia Type Ii

Isolated Focal Cortical Dysplasia Type Iib

Fcd Type Iib

Cortical Dysplasia, Taylor Type

Fcd Type Ii

Isolated Focal Cortical Dysplasia Type 2

Isolated Focal Cortical Dysplasia Type Iia

Fcd Type Iia

Isolated Focal Cortical Dysplasia

Epilepsy Due To Fcd

Focal Cortical Dysplasia 2

Cdtbc

Cdtd

Cortical Dysplasia Of Taylor With Balloon Cells

Cortical Dysplasia Of Taylor Without Balloon Cells

Fcd Iia

Fcd Iib

Fcord2a

Fcord2b

Focal Cortical Dysplasia, Type Iia

Focal Cortical Dysplasia, Type Iib

Focal Cortical Dysplasia Of Taylor Balloon Cell Type

FCDBC

Focal Cortical Dysplasia, Taylor Balloon Cell Type

Dysplasia, Cortical, Focal Type Ii

Focal Cortical Dysplasia Of Taylor, Type Iib

Tuberous Sclerosis 2

Tsc2 Angiomyolipomas, Renal, Modifier Of

TSC2

Tuberous Sclerosis

Tuberous Sclerosis-2

Tuberous Sclerosis, Type 2

Ts

Tuberous Sclerosis Complex

Tuberous Sclerosis 1

Tuberous Sclerosis Complex

Tuberous Sclerosis

Bourneville Syndrome

TSC1

Tuberose Sclerosis

Ts

Tuberous Sclerosis-1

Bourneville Disease

Tsc

Bourneville Phakomatosis

Cerebral Sclerosis

Sclerosis Tuberosa

Tuberous Sclerosis, Type 1

Tuberous Sclerosis

Tuberous Sclerosis Syndrome

Bourneville'S Disease

Epiloia

Cerebral Sclerosis

Tuberose Sclerosis

Tuberous Sclerosis 1

Bourneville Disease

Bourneville Phakomatosis

Pringle'S Disease

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease

Polycystic Kidney Disease 1

PKD1

Adpkd

Polycystic Kidney Disease, Adult, Type I

Apkd1

Potter Type Iii Polycystic Kidney Disease

Polycystic Kidney Disease, Adult

Potter Type Iii Polycystic Kidney Disease, Formerly

Polycystic Kidney Disease, Type 1

Adpkd1

Adult Polycystic Kidney Disease Type 1

Autosomal Dominant Polycystic Kidney Disease 1

Pkd-1

Polycystic Kidney Disease Adult

Polycystic Kidney Disease Type I

Polycystic Kidneys

Polycystic Kidney Disease, Adult Type I

Polycystic Kidney Type 1 Autosomal Dominant Disease

Kidney Disease, Polycystic, Type 1

Polycystic Kidney, Autosomal Dominant

Polycystic Kidney, Type 1 Autosomal Dominant Disease

Polycystic Kidney Diseases

Autosomal Dominant Polycystic Kidney Disease

Polycystic Kidney Disease, Adult Type

Adpkd

Polycystic Kidney Diseases

Polycystic Kidney, Autosomal Dominant

Congenital Biliary Ectasias

Polycystic Kidney And Hepatic Disease 1

Polycystic Kidney Disease, Autosomal Dominant

Kidney, Polycystic, Disease, Autosomal Dominant

Adult Polycystic Kidney Disease

Polycystic Kidney, Adult Type

Apckd - [Autosomal Polycystic Kidney Disease]

West Syndrome

Infantile Spasms

Infantile Spasms Syndrome

Infantile Spasm

X-Linked Infantile Spasm Syndrome

X-Linked Infantile Spasms

Epileptic Encephalopathy, Early Infantile, 1

Is

Tonic Spasms With Clustering, Arrest Of Psychomotor Development And Hypsarrhythmia On Eeg

West'S Syndrome

Spasms, Infantile

Is -[Infantile Spasm]

Salaam Spasm

Salaam Tic

Nervous System Disease

Abnormality Of The Nervous System

Nervous System Diseases

Nervous System Disorder

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

Bap1 Tumor Predisposition Syndrome

Bap1-Related Tumor Predisposition Syndrome

Common Syndrome

Bap1 Cancer Syndrome

Bap1-Tpds

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms

Tumor Predisposition Syndrome

Tumor Susceptibility Linked To Germline Bap1 Mutations

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms

Tumor Predisposition

Inherited Cancer-Predisposing Syndrome

Hereditary Cancer-Predisposing Syndrome

Angiomyolipoma

Angiomyolipoma Of Kidney

Subependymal Giant Cell Astrocytoma

Sega

Astrocytoma Subependymal Giant Cell

Subependymal Giant-Cell Astrocytoma

Polycystic Kidney Disease, Infantile Severe, With Tuberous Sclerosis

PKDTS

Tuberous Sclerosis/Polycystic Kidney Disease Contiguous Gene Syndrome

Polycystic Kidneys, Severe Infantile With Tuberous Sclerosis

Chromosome 16p13.3 Deletion Syndrome, Distal

Tuberous Sclerosis Polycystic Kidney Disease Contiguous Gene Syndrome

Autosomal Dominant Polycystic Kidney Disease Type 1 With Tuberous Sclerosis

Tsc2/Pkd1 Contiguous Gene Syndrome

Kidney Angiomyolipoma

Angiomyolipoma Of Kidney

Renal Angiomyolipoma

Peutz-Jeghers Syndrome

PJS

Polyposis, Hamartomatous Intestinal

Polyps-And-Spots Syndrome

Lentiginosis, Perioral

Periorificial Lentiginosis Syndrome

Hamartomatous Intestinal Polyposis

Hamartomatous Polyp

Colonic Hamartomatous Polyp

Gastric Peutz-Jeghers Polyp

Peutz Jeghers Colon Polyp

Peutz Jeghers Polyp

Peutz-Jeghers Polyp Of Small Intestine

Peutz-Jeghers Small Bowel Hamartoma

Peutz Jeghers Polyposis

Intestinal Polyposis-Cutaneous Pigmentation Syndrome

Peutz-Jeghers Polyposis

Polyposis, Intestinal, Ii

Intestinal Hamartomatous Polyposis

Peutz-Jeghers Polyp

Peutz-Jeghers Polyp Of The Stomach

Peutz Jehgers Polyp

Peutz-Jeghers Polyps Of Small Bowel

Ganglioglioma

Childhood Ganglioglioma

Adult Ganglioglioma

Cns Ganglioglioma

Mixed Cell Tumors Containing Both Neural Ganglionic Cells And Neural Glial Cell Components

Cystic Kidney Disease

Renal Cyst

Simple Renal Cyst

Kidney Cysts

Kidney Diseases, Cystic

Renal Cysts

Kidney Cyst

Cystic Kidney

Congenital Cystic Kidney Disease

Cystic Kidney Diseases

Bosniak 1 Cyst

Subependymal Glioma

Mixed Subependymoma-Ependymoma

Subependymal Astrocytoma

Who Grade I Ependymal Tumor

Glioma, Subependymal

Benign Ependymoma

Ependymoma

Epithelial Ependymoma

Who Grade Ii Ependymal Tumor

Myxopapillary Ependymoma

Kidney Benign Neoplasm

Renal And Ureteral Tumor

Benign Kidney Neoplasm

Adult Hepatocellular Carcinoma

Adult Primary Hepatocellular Carcinoma

Adult Hepatoma

Adult Hcc

Lymphangiomatosis
Subependymoma

Subependymal Astrocytoma

Subependymal Glioma

Congenital Heart Defects, Hamartomas Of Tongue, And Polysyndactyly

Ostravik-Lindemann-Solberg Syndrome

CHDTHP

Heart Defect-Tongue Hamartoma-Polysyndactyly Syndrome

Orstavik Lindemann Solberg Syndrome

Heart Defect - Tongue Hamartoma - Polysyndactyly Syndrome

Heart Defect, Tongue Hamartoma And Polysyndactyly

Hamartoma

Polycystic Kidney Disease

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant

Perivascular Epithelioid Cell Tumor

Pecoma

Perivascular Epithelioid Cell Neoplasms

Neoplasm With Perivascular Epithelioid Cell Differentiation

Epilepsy

Epilepsy Syndrome

Epileptic Syndrome

Epilepsies

Symptomatic Epilepsies

Post Traumatic Epilepsy

Traumatic Epilepsy

Traumatic Epileptic

Epilepsy Due To Hippocampal Sclerosis

Epilepsy With Ammon'S Horn Sclerosis

Epilepsy Due To Cortical Dysplasia

Epilepsy Due To Neuronal Migration Disorders

Lung Disease

Lung Diseases

Disorder Of Lung

Abnormality Of The Lung

Cowden Syndrome 1

Bannayan-Riley-Ruvalcaba Syndrome

Pten Hamartoma Tumor Syndrome

Lhermitte-Duclos Disease

Bannayan-Zonana Syndrome

Phts

Riley-Smith Syndrome

Bzs

Ruvalcaba-Myhre-Smith Syndrome

Multiple Hamartoma Syndrome

Rmss

Brrs

Dysplastic Gangliocytoma Of The Cerebellum

CWS1

Cs

Cd

Mham

Pten Hamartoma Tumor Syndrome With Granular Cell Tumor

Macrocephaly Multiple Lipomas And Hemangiomata

Bannayan-Ruvalcaba-Riley Syndrome

Myhre-Riley-Smith Syndrome

LDD

Cerebelloparenchymal Disorder Vi

Hamartoma Syndrome, Multiple

Bbrs

Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata

Macrocephaly, Multiple Lipomas, And Hemangiomata

Macrocephaly Pseudopapilledema And Multiple Hemangiomas

Ruvalcaba -Myhre-Smith Syndrome

Ruvalcaba-Myhre Syndrome

Cowden Disease

Macrocephaly Pseudopapilledema And Multiple Hemangiomata

Cerebellar Granule Cell Hypertrophy And Megalencephaly

Cpd6

Pten Hamartoma Tumor Syndromes

Cowden Syndrome, Type 1

Hepatic Angiomyolipoma
Epithelioid Type Angiomyolipoma

Epithelioid Angiomyolipoma

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Fallopian Tube Leiomyoma
Cowden Syndrome

Cowden Disease

Multiple Hamartoma Syndrome

Cowden'S Disease

Lhermitte-Duclos Disease

Cd

Cs

Mham

Dysplastic Gangliocytoma Of Cerebellum

Cowden'S Syndrome

Hamartoma Syndrome, Multiple

Leiomyoma

Leiomyomatous Neoplasm

Leiomyomatous Tumor

Leiomyomas

Fibroid Tumor

Uterine Fibroids

Fragile X Syndrome

FXS

Martin-Bell Syndrome

Fraxa Syndrome

Marker X Syndrome

X-Linked Mental Retardation And Macroorchidism

Fragile X Mental Retardation Syndrome

Fra Syndrome

Mental Retardation, X-Linked, Associated With Marxq28

X-Linked Intellectual Disability And Macroorchidism

Frax Syndrome

Symptomatic Form Of Fragile X Syndrome In Female Carriers

Fragile-X Syndrome

Fraxe Syndrome

Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease

Autosomal Recessive Polycystic Kidney Disease

Arpkd

Polycystic Kidney Disease, Autosomal Recessive

Polycystic Kidney And Hepatic Disease 1

Pkhd1

PKD4

Polycystic Kidney Disease 4 With Or Without Hepatic Disease

Polycystic Kidney Disease, Infantile, Type I

Polycystic Kidney Disease, Infantile Type

Polycystic Kidney, Autosomal Recessive

Pkd3, Formerly

Polycystic Kidney Disease 4, With Or Without Hepatic Disease

Arpkd/Chf

Ar-Pkd

Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease

Infantile Polycystic Kidney Disease Type I

Pkd3

Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease

Polycystic Kidney Disease 3, Autosomal Dominant

Optic Nerve Astrocytoma

Astrocytic Tumor Of Optic Nerve

Optic Tract Astrocytoma

Visual Pathway Astrocytoma

Von Hippel-Lindau Syndrome

Von Hippel-Lindau Disease

Vhl

Vhl Syndrome

VHLS

Von Hippel-Lindau Syndrome, Modifier Of

Hippel Lindau Syndrome

Angiomatosis Retinae

Cerebelloretinal Angiomatosis, Familial

Hippel-Lindau Disease

Familial Cerebelloretinal Angiomatosis

Lindau Disease

VHLD

Perivascular Tumor

Malignant Perivascular Cancer

Kidney Cancer

Renal Cancer

Renal Carcinoma

Kidney Neoplasm

Malignant Neoplasm Of Kidney Except Pelvis

Malignant Tumour Of Kidney

Kidney Neoplasms

Cancer, Kidney

Cancer, Renal

Malignant Neoplasm Of Kidney

Renal Cell Carcinoma

Heart Cancer

Malignant Neoplasm Of Heart

Heart Neoplasm

Cardiac Tumor

Malignant Cardiac Tumor

Tumour Of Heart

Heart Neoplasms

Cardiac Carcinoma

Neurofibromatosis, Type I

Von Recklinghausen Disease

Neurofibromatosis 1

Neurofibromatosis, Type 1

NF1

Neurofibromatosis, Peripheral Type

Neurofibromatosis Type I

Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion

Familial Spinal Neurofibromatosis

Fsnf

Peripheral Neurofibromatosis

Von Recklinghausen'S Neurofibromatosis

Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion

Neurofibromatosis Peripheral Type

Von Recklinghausen Syndrome

Neurofibromatosis Type 1

Von Recklinghausen Neuropathy

Nf1 - [Neurofibromatosis Type 1]

Recklinghausen Disease

Lymphoid Interstitial Pneumonia

Lymphocytic Interstitial Pneumonia

Lip Disease

Lip Diseases

LIP

Disease Of Lips

Birt-Hogg-Dube Syndrome

Hornstein-Knickenberg Syndrome

Fibrofolliculomas With Trichodiscomas And Acrochordons

BHD

Birt-Hogg-Dubé Syndrome

Multiple Fibrofolliculoma Familial

Bhd Syndrome

Birt Hogg Dube Syndrome

Hornstein-Birt-Hogg-Dubé Syndrome

Multiple Fibrofolliculomas

Hemangioma

Hemangiomas

Fallopian Tube Benign Neoplasm
Corneal Dystrophy, Fleck

Fleck Corneal Dystrophy

Fcd

CFD

Corneal Fleck Dystrophy

Francois-Neetens Speckled Corneal Dystrophy

Corneal Dystrophy, Francois-Neetens Speckled Or Flecked

Corneal Dystrophy Francois-Neetens Speckled Or Flecked

Dystrophy, Corneal, Fleck

Proteus Syndrome

Proteus Syndrome, Somatic

Partial Gigantism-Nevi-Hemihypertrophy-Macrocephaly Syndrome

Gigantism, Partial, Of Hands And Feet, Nevi, Hemihypertrophy, And Macrocephaly

Wiedemann'S Syndrome

Hemihypertrophy And Macrocephaly

Partial Gigantism Of Hands And Feet, Nevi, Hemihypertrophy, Macrocephaly

Ps

PROTEUSS

Partial Gigantism Of Hands And Feet Nevi Hemihypertrophy And Macrocephaly

Multilocular Clear Cell Renal Cell Carcinoma

Cystadenocarcinoma Of Kidney

Renal Cystadenocarcinoma

Renal Cell Carcinoma, Nonpapillary

Renal Cell Carcinoma

RCC

Nonpapillary Renal Cell Carcinoma

Clear Cell Renal Cell Carcinoma

Hypernephroma

Adenocarcinoma Of Kidney

Renal Carcinoma, Chromophobe, Somatic

Clear Cell Carcinoma Of Kidney

Clear-Cell Metastatic Renal Cell Carcinoma

Clear Cell Renal Carcinoma

Renal Cell Carcinoma, Somatic

Conventional Renal Cell Carcinoma

Conventional Renal Cell Carcinoma

Renal Clear Cell Carcinoma

Ccrcc

Hereditary Clear Cell Renal Cell Carcinoma

Carcinoma, Renal Cell

Renal Cell Carcinoma, Clear Cell, Somatic

Renal Cell Carcinoma, Clear Cell

Clear Cell Kidney Carcinoma

Clear Cell Rcc

Cystic-Multilocular Variant

Clear Cell Renal Cell Adenocarcinoma

Hereditary Clear Cell Renal Cell Adenocarcinoma

Common Renal Cell Carcinoma

Crcc

Renal Cell Carcinoma Non-Papillary

Carcinoma Renal Cell

Renal Cell Cancer

Carcinoma, Renal Cell, Nonpapillary

Low Grade Glioma

Benign Glioma

Central Nervous System Benign Neoplasm

Benign Neoplasm Of The Central Nervous System

Kidney Disease

Renal Failure

Kidney Failure

Kidney Diseases

Nephropathy

Abnormality Of The Kidney

Impaired Renal Function Disease

Renal Anomaly

Kidney Dysfunction

Renal Disease

Nephropathies

Renal Failure Adverse Event

Abnormal Renal Function

Hereditary Renal Cell Carcinoma
Neurodegeneration With Brain Iron Accumulation

Nbia

Neurodegeneration With Brain Iron Accumulation Disorders

Neurodegeneration, With Brain Iron Accumulation

Angiolipoma
Obstructive Hydrocephalus
Spinal Cord Disease

Spinal Cord Diseases

Myelopathy

Bone Marrow Diseases

Connective Tissue Benign Neoplasm

Soft Tissue Neoplasms

Mesenchymal Tissue Neoplasm

Neoplasm Of Soft Tissue

Neoplasm Of Soft Tissues

Soft Tissue Benign Neoplasm

Tumor Of The Soft Tissue

Soft Tissue Neoplasm

Cowden Syndrome 4

CWS4

Cowden Syndrome, Type 4

Vascular Cancer

Blood Vessel Tumors

Malignant Vascular Neoplasm

Renal Vein Leiomyosarcoma

Vascular Neoplasms

Blood Vessel Neoplasm

Blood Vessel Tumor

Blood Vessel Tumour Disorder

Haemangiomatous Tumour

Leiomyosarcoma Of The Renal Vein

Malignant Great Vessel Tumor

Malignant Tumor Of Pulmonary Artery

Malignant Tumor Of Pulmonary Vein

Malignant Vascular Tumor

Neoplasm Of Great Vessel

Pulmonary Artery Malignant Neoplasm

Pulmonary Vein Malignant Neoplasm

Vascular Tissue Neoplasm

Vascular Tumors

Blood Vessel Cancer

Neoplasms, Vascular Tissue

Malignant Neoplasm Of Great Vessels

Uterine Benign Neoplasm
Glioblastoma

Glioblastoma Multiforme

Gbm

Adult Glioblastoma Multiforme

Grade Iv Adult Astrocytic Tumor

Primary Glioblastoma Multiforme

Spongioblastoma Multiforme

Adult Glioblastoma

Primary Glioblastoma

Hepatocellular Carcinoma

Liver Cancer

Primary Liver Cancer

HCC

Hepatoma

Malignant Neoplasm Of Liver

Liver Neoplasms

Cancer, Hepatocellular

Liver Cell Carcinoma

Lcc

Hepatoblastoma, Somatic

Hepatic Cancer

Primary Malignant Neoplasm Of Liver

Rare Tumor Of Liver And Intrahepatic Biliary Tract

Hepatocellular Carcinoma, Somatic

Hepatocellular Carcinoma, Childhood Type, Somatic

Hepatocellular Cancer, Somatic

Ca Liver - Primary

Hepatic Neoplasm

Malignant Hepato-Biliary Neoplasm

Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

Malignant Neoplasm Of Liver, Primary

Malignant Tumor Of Liver

Neoplasm Of Liver

Non-Resectable Primary Hepatic Malignant Neoplasm

Resectable Malignant Neoplasm Of Liver

Resectable Malignant Neoplasm Of The Liver

Primary Liver Carcinoma

Primary Malignant Liver Neoplasm

Primary Cancer Of Liver

Primary Tumor Of The Liver

Rare Tumor Of Liver And Ibt

Hepatocellular Cancer

Neoplasm Of The Liver

Carcinoma, Hepatocellular

Hepatomas

Liver Neoplasm

Liver Carcinoma

Liver And Intrahepatic Biliary Tract Carcinoma

Malignant Hepatobiliary Neoplasm

Adult Primary Hepatocellular Carcinoma

Hepatoblastoma

Carcinoma Of Liver

Malignant Liver Tumour

Malignant Hepatic Tumour

Hypomelanosis Of Ito

Incontinentia Pigmenti Achromians

Nevus Of Ito

Ipa

Ito Hypomelanosis

Ito

Pigmentation Disorders

HMI

Incontinentia Pigmenti, Type I, Formerly

Ip1, Formerly

Bloch-Siemans Syndrome

Incontinentia Pigmenti Achromians Syndrome

Ito'S Nevus

Incontinentia Pigmenti Type 1

Nevi Of Ito

Nevus Fuscocaeruleus Acromiodeltoideus

Bloch Sulzberger Syndrome

Skin Pigmentation Disorder

Pitt-Hopkins-Like Syndrome 1

Cortical Dysplasia-Focal Epilepsy Syndrome

CDFES

PTHSL1

Cdfe Syndrome

Pitt-Hopkins Like Syndrome 1

Pitt-Hopkins-Like Syndrome-1

Cntnap2-Related Developmental And Epileptic Encephalopathy

Cntnap2-Related Dee

Mesh

D006985

Mesh

D008607

Sturge-Weber Syndrome

SWS

Encephalotrigeminal Angiomatosis

Encephalofacial Angiomatosis

Sturge-Weber-Dimitri Syndrome

Sturge-Weber-Krabbe Syndrome

Fourth Phacomatosis

Leptomeningeal Angiomatosis

Meningeal Capillary Angiomatosis

Sturge-Weber-Krabbe Angiomatosis

Sturge-Weber Syndrome, Somatic, Mosaic

Sws Type I - Facial And Leptomeningeal Angiomas

Sws Type Ii - Facial Angioma Alone, No Cns Involvement

Sws Type Iii - Isolated Leptomeningeal Angiomas

Sturge Weber Syndrome

Angiomatosis Aculoorbital-Thalamic Syndrome

Encephalofacial Hemangiomatosis

Encephalofacial Hemangiomatosis Syndrome

Meningo-Oculo-Facial Angiomatosis

Meningofacial Angiomatosis-Cerebral Calcification Syndrome

Neuroretinoangiomatosis

Phakomatosis, Sturge-Weber

Weber-Sturge-Dimitri Syndrome

Reproductive Organ Benign Neoplasm
Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Gangliocytoma

Ganglioneuroma

Gangliocytoma Of Central Nervous System

Pervasive Developmental Disorder

Pervasive Development Disorder

Pervasive Developmental Disorders

Pervasive Child Development Disorders

Autistic Behavior

Autism Spectrum Disorders

Polycystic Liver Disease 1 With Or Without Kidney Cysts

Polycystic Liver Disease 1

PCLD1

Cyst

Liver Disease, Polycystic, Type 1

Polycystic Liver Disease

Endometrial Cancer

Endometrial Carcinoma

Endometrial Neoplasm

Malignant Neoplasm Of Endometrium

Endometrioid Carcinoma

Endometrial Neoplasms

Carcinoma, Endometrioid

Endometrial Cancer, Familial

Endometrial Carcinoma, Somatic

Endometrial Cancer, Susceptibility To

Endometrial Ca

Malignant Endometrial Neoplasm

Neoplasm Of Endometrium

Primary Malignant Neoplasm Of Endometrium

Tumor Of Endometrium

Carcinoma Of The Endometrium

Endometrioid Carcinoma Of Female Reproductive System

ENDMC

Carcinoma Endometrioid

Endometrial Cancers

Cancer, Endometrial

Uterine Corpus Cancer

Developmental And Epileptic Encephalopathy 87

DEE87

Epileptic Encephalopathy, Early Infantile, 87

Eiee87

Developmental And Epileptic Encephalopathy, 87

Early Infantile Epileptic Encephalopathy 87

Uterus Perivascular Epithelioid Cell Tumor

Uterine Corpus Pecoma

Stromal Dystrophy
Liver Lipoma

Hepatic Lipoma

Lipoma Of The Liver

Respiratory System Benign Neoplasm
Specific Developmental Disorder
Cell Type Benign Neoplasm
Polymicrogyria, Bilateral Perisylvian, X-Linked

Bilateral Perisylvian Polymicrogyria

Polymicrogyria, Bilateral Perisylvian

Pmgx

Perisylvian Syndrome, Congenital Bilateral

Cbps

Congenital Bilateral Perisylvian Syndrome

Perisylvian Syndrome

BPPX

Bpp

Medulloblastoma

MDB

Cpnet

Localized Primitive Neuroectodermal Tumor

Classic Medulloblastoma

Medulloblastoma Predisposition Syndrome

Medulloblastoma, Somatic

Brain Medulloblastoma

Cns Pnet

Infratentorial Primitive Neuroectodermal Tumor

Neuroectodermal Tumors, Primitive

Medulloblastomas

Desmoplastic Medulloblastoma

Medulloblastoma, With Extensive Nodularity

Medulloblastoma Of Unspecified Site

Medullomyoblastoma Of Unspecified Site

Lennox-Gastaut Syndrome

Lennox Syndrome

Encephalopathy Of Childhood

Epileptic Encephalopathy Lennox-Gastaut Type

Childhood Epileptic Encephalopathy With Diffuse Slow Spikes And Waves

Lgs

Periventricular Nodular Heterotopia

Periventricular Heterotopia

Pvnh

Familial Nodular Heterotopia

Heterotopia, Periventricular

Periventricular Heterotopia, X-Linked

Dravet Syndrome

Severe Myoclonic Epilepsy Of Infancy

Severe Myoclonic Epilepsy In Infancy

Smei

Epileptic Encephalopathy, Early Infantile, 6

DRVT

Developmental And Epileptic Encephalopathy 6a

Dee6a

Eiee6

Developmental And Epileptic Encephalopathy, 6

Dee6

Developmental And Epileptic Encephalopathy 6

Early Infantile Epileptic Encephalopathy 6

Myoclonic Epilepsy, Severe, Of Infancy

Sme

Severe Myoclonus Epilepsy Of Infancy

Borderline Smei

Smeb

Smeb-M

Smeb-O

Smeb-Sw

Smei-Borderland

Smei-Borderland More Than One Feature

Smei-Borderland-Myoclonic Seizures

Smei-Borderland-Spike Wave

Intractable Childhood Epilepsy With Generalized Tonic-Clonic Seizures

ICEGTC

Infantile Severe Myoclonic Epilepsy

Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures

Polycystic Liver Disease

Autosomal Dominant Polycystic Liver Disease

Isolated Polycystic Liver Disease

Pcld

Congenital Cystic Liver Disease

Congenital Hepatic Cyst

Fibrocystic Liver Disease

Isolated Autosomal Dominant Polycystic Liver Disease

Adpcld

Liver Disease, Polycystic

Multiple Cysts Of Liver

Pld - [Polycystic Liver Disease]

Polycystic Liver Disorder

Polycystic Liver

Congenital Polycystic Disease Of Liver

Congenital Polycystic Liver Disease

Rasopathy

Ras/Mitogen-Activated Protein Kinase Syndrome

Developmental And Epileptic Encephalopathy

Encephalopathy, Developmental And Epileptic

Type 2 Diabetes Mellitus

Insulin Resistance

NIDDM

Type 2 Diabetes

Diabetes Mellitus, Non-Insulin-Dependent

T2D

Noninsulin-Dependent Diabetes Mellitus

Diabetes Mellitus, Type Ii

Maturity-Onset Diabetes

Insulin Resistance, Severe, Digenic

Diabetes Mellitus, Type 2

Diabetes Mellitus, Noninsulin-Dependent

Diabetes Mellitus, Noninsulin-Dependent, Association With

Diabetes Mellitus, Noninsulin-Dependent, Late Onset

Hypertension, Insulin Resistance-Related, Susceptibility To

Insulin Resistance, Susceptibility To

Non-Insulin-Dependent Diabetes Mellitus

Type Ii Diabetes Mellitus

Adult-Onset Diabetes Mellitus

Maturity-Onset Diabetes Mellitus

Diabetes Mellitus Type 2

Type Ii Diabetes

Type 2 Diabetes Mellitus, Susceptibility To

Diabetes, Type 2

Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

Diabetes Mellitus, Type 2, Susceptibility To

Diabetes Mellitus, Noninsulin-Dependent, 2

Diabetes Mellitus, Type Ii, Susceptibility To

Hypertension, Insulin Resistance-Related

Adult-Onset Diabetes

Aodm

Diabetes Mellitus, Adult-Onset

Diabetes Mellitus Type Ii

Diabetes Mellitus Type 2, Susceptibility To

Diabetes, Type Ii, Susceptibility To

Diabetes Type 2

Diabetes Mellitus

Adult Onset Diabetes

Maturity Onset Diabetes

Nonketotic Diabetes

Non-Insulin Dependent Diabetes Mellitus

T2dm - [Type 2 Diabetes Mellitus]

Niddm - [Non Insulin Dependent Diabetes Mellitus]

Dm2

Dm Type Ii

Diabetic Type 2

Insulin Requiring Type 2 Diabetes

Noninsulin Dependent Diabetes

Non-Insulin-Dependent Diabetes Mellitus Without Complications

Diabetes Due To Insulin Secretory Defect

Diabetes Mellitus Due To Insulin Secretory Defect

Non-Insulin-Dependent Diabetes Of The Young

Senile Diabetes

Nonketotic Hyperglycaemia

Stable Diabetes

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder

ADHD

Attention Deficit Disorder

Attention Deficit-Hyperactivity Disorder, Susceptibility To

Attention Deficit Disorder With Hyperactivity

Hyperkinetic Disorder

Hyperactivity Of Childhood

Attention-Deficit/Hyperactivity Disorder

Add

Addh

Attention Deficit

Attention Deficit Disorder Of Childhood With Hyperactivity

Attention Deficit Disorder With Hyperactivity Syndrome

Hyperkinetic Syndrome

Attention-Deficit Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

Disturbance Of Activity And Attention

Disorder Of Activity And Attention

Adhd - [Attention Deficit Hyperactivity Disorder]

Hyperkinetic Disorders

Disorder Of Activity And Attention With Hyperkinesia

Attention Deficit Syndrome With Hyperactivity

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy

Benign Rolandic Epilepsy

Epilepsy, Rolandic

Bcects

Benign Childhood Epilepsy With Centrotemporal Spike

Sylvan Seizures

Becrs

Bects

Bre

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Benign Familial Epilepsy Of Childhood With Rolandic Spikes

Centrotemporal Epilepsy

Alzheimer Disease, Familial, 1

Alzheimer Disease

Alzheimer'S Disease

Presenile And Senile Dementia

AD1

Alzheimer Disease, Susceptibility To

Alzheimer Disease, Late-Onset, Susceptibility To

Alzheimer Disease 1, Familial

AD

Familial Alzheimer Disease

Alzheimer Disease, Late-Onset

Alzheimers Dementia

Alzheimer Dementia

Alzheimer Sclerosis

Alzheimer Syndrome

Alzheimer-Type Dementia

Dat

Primary Senile Degenerative Dementia

Sdat

Alzheimer Disease 1

Autosomal Dominant Alzheimer Disease

Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

Late Onset Alzheimer Disease

Alzheimers Disease

Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

Late-Onset Alzheimers Disease

Alzheimer'S Disease Pathway Kegg

Dementia Due To Alzheimer'S Disease

Alzheimer Disease Type 1

Alzheimers

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Felis catus TSC2 VGNC VGNC:66606
Mus musculus TSC2 MGD MGI:102548
Macaca mulatta TSC2 VGNC VGNC:78659
Bos taurus TSC2 VGNC VGNC:36408
Rattus norvegicus TSC2 RGD RGD:3908
Canis familiaris TSC2 VGNC VGNC:47891
Others TSC2 NCBI