1. Gene
  2. KRT3 - keratin 3 Gene

KRT3 - keratin 3 Gene

中文名称:角蛋白 3

种属: Homo sapiens

同用名: K3; CK3; MECD2

基因 ID: 3850 | 基因类型: protein coding

关于 KRT3

Cytogenetic location: 12q13.13 Genomic coordinates (GRCh38): 12:52,789,685-52,796,117 (from NCBI)

This gene has 1 transcript (splice variant), 72 orthologues, 68 paralogues and is associated with 3 phenotypes. Low expression observed in reference dataset.

功能概要

该基因编码的蛋白质是角蛋白基因家族的一员。 II 型细胞角蛋白由碱性或中性蛋白组成,这些蛋白排列成对异型角蛋白链,在单层和复层上皮组织分化过程中共同表达。这种 II 型细胞角蛋白与家族成员 KRT12 在角膜上皮细胞中特异性表达,这些基因的突变与 Meesmann 角膜营养不良有关。 II 型细胞角蛋白聚集在染色体 12q12-q13 的区域中。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]

KRT3 基因产物(1)

mRNA Protein Name
NM_057088.3 NP_476429.2 keratin, type II cytoskeletal 3
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in intermediate filament cytoskeleton organization IMP
IMP: 通过突变表型推断
9171831 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

KRT3 蛋白结构

Filament

Filament: Intermediate filament protein (197 - 512)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 628 a.a.
蛋白主名 其他名称

keratin, type II cytoskeletal 3

65 kDa cytokeratin

KRT3 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
KRT3 P12035 g4xuv3_human Homo sapiens G4XUV3 32296183
种属内
KRT3 P12035 g4xuv3_human Homo sapiens G4XUV3 32296183
种属内
KRT3 P12035 KRT37 Homo sapiens O76014 32296183
种属内
KRT3 P12035 KRT34 Homo sapiens O76011 32296183
种属内
KRT3 P12035 KRT34 Homo sapiens O76011 32296183
种属内
KRT3 P12035 KRT38 Homo sapiens O76015 32296183
种属内
KRT3 P12035 KRT38 Homo sapiens O76015 32296183
种属内
KRT3 P12035 KRT33B Homo sapiens Q14525 32296183
种属内
KRT3 P12035 KRT33B Homo sapiens Q14525 32296183
种属内
KRT3 P12035 KRT33B Homo sapiens Q14525 32296183
种属内
KRT3 P12035 KRT35 Homo sapiens Q92764 32296183
种属内
KRT3 P12035 KRT35 Homo sapiens Q92764 32296183
种属内
KRT3 P12035 KRT35 Homo sapiens Q92764 32296183
种属内
KRT3 P12035 KRTAP13-2 Homo sapiens Q52LG2 32296183
种属内
KRT3 P12035 KRTAP13-2 Homo sapiens Q52LG2 32296183
种属内
KRT3 P12035 KRTAP13-2 Homo sapiens Q52LG2 32296183
种属内
KRT3 P12035 KRT39 Homo sapiens Q6A163 32296183
种属内
KRT3 P12035 KRT39 Homo sapiens Q6A163 32296183
种属内
KRT3 P12035 KRT39 Homo sapiens Q6A163 32296183
种属内
KRT3 P12035 KRT36 Homo sapiens O76013-2 32296183
种属内
KRT3 P12035 KRT36 Homo sapiens O76013-2 32296183
种属内
KRT3 P12035 KRT25 Homo sapiens Q7Z3Z0 32296183
种属内
KRT3 P12035 KRT25 Homo sapiens Q7Z3Z0 32296183
种属内
KRT3 P12035 KRT25 Homo sapiens Q7Z3Z0 32296183
种属内
KRT3 P12035 KRT28 Homo sapiens Q7Z3Y7 32296183
种属内
KRT3 P12035 KRT28 Homo sapiens Q7Z3Y7 32296183
种属内
KRT3 P12035 KRT28 Homo sapiens Q7Z3Y7 32296183
种属内
KRT3 P12035 LHX3 Homo sapiens Q9UBR4-2 32296183
种属内
KRT3 P12035 LHX3 Homo sapiens Q9UBR4-2 32296183
种属内
KRT3 P12035 LHX3 Homo sapiens Q9UBR4-2 32296183
种属内
KRT3 P12035 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
KRT3 P12035 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
KRT3 P12035 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
KRT3 P12035 KRT26 Homo sapiens Q7Z3Y9 32296183
种属内
KRT3 P12035 KRT26 Homo sapiens Q7Z3Y9 32296183
种属内
KRT3 P12035 KRT26 Homo sapiens Q7Z3Y9 32296183
种属内
KRT3 P12035 KIFC3 Homo sapiens Q9BVG8-5 32296183
种属内
KRT3 P12035 KIFC3 Homo sapiens Q9BVG8-5 32296183
种属内
KRT3 P12035 KIFC3 Homo sapiens Q9BVG8-5 32296183
种属内
KRT3 P12035 TRIM54 Homo sapiens Q9BYV2 32296183
种属内
KRT3 P12035 TRIM54 Homo sapiens Q9BYV2 32296183
种属内
KRT3 P12035 TRIM54 Homo sapiens Q9BYV2 32296183
种属内
KRT3 P12035 HAUS1 Homo sapiens Q96CS2 32296183
种属内
KRT3 P12035 HAUS1 Homo sapiens Q96CS2 32296183
种属内
KRT3 P12035 HAUS1 Homo sapiens Q96CS2 32296183
种属内
KRT3 P12035 SAPCD2 Homo sapiens Q86UD0 32296183
种属内
KRT3 P12035 SAPCD2 Homo sapiens Q86UD0 32296183
种属内
KRT3 P12035 SAPCD2 Homo sapiens Q86UD0 32296183
种属内
KRT3 P12035 C3orf62 Homo sapiens Q6ZUJ4 32296183
种属内
KRT3 P12035 C3orf62 Homo sapiens Q6ZUJ4 32296183
种属内
KRT3 P12035 C3orf62 Homo sapiens Q6ZUJ4 32296183
种属内
KRT3 P12035 KRT75 Homo sapiens O95678 32296183
种属内
KRT3 P12035 KRT75 Homo sapiens O95678 32296183
种属内
KRT3 P12035 KRT24 Homo sapiens Q2M2I5 32296183
种属内
KRT3 P12035 KRT24 Homo sapiens Q2M2I5 32296183
种属内
KRT3 P12035 KRT24 Homo sapiens Q2M2I5 32296183
种属内
KRT3 P12035 KRT27 Homo sapiens Q7Z3Y8 32296183
种属内
KRT3 P12035 KRT27 Homo sapiens Q7Z3Y8 32296183
种属内
KRT3 P12035 KRT27 Homo sapiens Q7Z3Y8 32296183
种属内
KRT3 P12035 NUP62 Homo sapiens P37198 32296183
种属内
KRT3 P12035 NUP62 Homo sapiens P37198 32296183
种属内
KRT3 P12035 NUP62 Homo sapiens P37198 32296183
种属内
KRT3 P12035 KRT16 Homo sapiens P08779 32296183
种属内
KRT3 P12035 KRT16 Homo sapiens P08779 32296183
种属内
KRT3 P12035 TRAF1 Homo sapiens Q13077 32296183
种属内
KRT3 P12035 TRAF1 Homo sapiens Q13077 32296183
种属内
KRT3 P12035 TRAF1 Homo sapiens Q13077 32296183
种属内
KRT3 P12035 SPAG5 Homo sapiens Q96R06 32296183
种属内
KRT3 P12035 SPAG5 Homo sapiens Q96R06 32296183
种属内
KRT3 P12035 SPAG5 Homo sapiens Q96R06 32296183
种属内
KRT3 P12035 OIP5 Homo sapiens O43482 32296183
种属内
KRT3 P12035 OIP5 Homo sapiens O43482 32296183
种属内
KRT3 P12035 KRT14 Homo sapiens P02533 32296183
种属内
KRT3 P12035 KRT14 Homo sapiens P02533 32296183
种属内
KRT3 P12035 TRIM27 Homo sapiens P14373 32296183
种属内
KRT3 P12035 TRIM27 Homo sapiens P14373 32296183
种属内
KRT3 P12035 TRIM27 Homo sapiens P14373 32296183
种属内
KRT3 P12035 HGS Homo sapiens O14964 32296183
种属内
KRT3 P12035 HGS Homo sapiens O14964 32296183
种属内
KRT3 P12035 LURAP1 Homo sapiens Q96LR2 32296183
种属内
KRT3 P12035 LURAP1 Homo sapiens Q96LR2 32296183
种属内
KRT3 P12035 LURAP1 Homo sapiens Q96LR2 32296183
种属内
KRT3 P12035 KRT20 Homo sapiens P35900 32296183
种属内
KRT3 P12035 KRT19 Homo sapiens P08727 32296183
种属内
KRT3 P12035 KRT19 Homo sapiens P08727 32296183
种属内
KRT3 P12035 ZNF426 Homo sapiens Q9BUY5 32296183
种属内
KRT3 P12035 ZNF426 Homo sapiens Q9BUY5 32296183
种属内
KRT3 P12035 ZNF426 Homo sapiens Q9BUY5 32296183
种属内
KRT3 P12035 DEUP1 Homo sapiens Q05D60 32296183
种属内
KRT3 P12035 DEUP1 Homo sapiens Q05D60 32296183
种属内
KRT3 P12035 DEUP1 Homo sapiens Q05D60 32296183
种属内
KRT3 P12035 CCDC197 Homo sapiens Q8NCU1 32296183
种属内
KRT3 P12035 CCDC197 Homo sapiens Q8NCU1 32296183
种属内
KRT3 P12035 CCDC197 Homo sapiens Q8NCU1 32296183
种属内
KRT3 P12035 KRT31 Homo sapiens Q15323 32296183
种属内
KRT3 P12035 KRT31 Homo sapiens Q15323 32296183
种属内
KRT3 P12035 KRT31 Homo sapiens Q15323 32296183
种属内
KRT3 P12035 PLEKHG4 Homo sapiens Q58EX7 32296183
种属内
KRT3 P12035 PLEKHG4 Homo sapiens Q58EX7 32296183
种属内
KRT3 P12035 PLEKHG4 Homo sapiens Q58EX7 32296183
种属内
KRT3 P12035 BPIFA1 Homo sapiens Q9NP55 32296183
种属内
KRT3 P12035 BPIFA1 Homo sapiens Q9NP55 32296183
种属内
KRT3 P12035 BPIFA1 Homo sapiens Q9NP55 32296183
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
Corneal Dystrophy, Meesmann, 2

Meesmann Corneal Dystrophy 2

MECD2

Corneal Dystrophy, Meesmann 2

Corneal Dystrophy, Meesmann, 1

Meesmann Corneal Dystrophy

Mecd

Corneal Dystrophy, Meesmann Epithelial

Juvenile Hereditary Epithelial Dystrophy

Corneal Dystrophy, Juvenile Epithelial Of Meesmann

MECD1

Meesmann Corneal Dystrophy 1

Meesmann Corneal Epithelial Dystrophy

Meesmann Epithelial Corneal Dystrophy

Corneal Dystrophy, Juvenile Epithelial, Of Meesmann

Stocker-Holt Dystrophy

Meesman Dystrophy

Meesman'S Corneal Dystrophy

Juvenile Hereditary Epithelial Dystrophy Of Meesmann

Corneal Dystrophy, Meesmann 1

Juvenile Epithelial Corneal Dystrophy Of Meesmann

Mcd

Dystrophy, Corneal, Meesmann

Corneal Dystrophy
Corneal Disease

Corneal Diseases

Corneal Disorders

Keratoconus

Kc

Conical Cornea

Noninflammatory Corneal Thining

Bulging Cornea

Cornea Conical

Acquired Conus Of Cornea

Cicatricial Entropion
Astigmatism
Corneal Endothelial Dystrophy

Congenital Hereditary Endothelial Dystrophy Of Cornea

Chandler Syndrome

CHED

Chandler'S Syndrome

Endothelial Corneal Dystrophy

Ched2

Maumenee Corneal Dystrophy

Corneal Dystrophy, Congenital Hereditary Endothelial

Dystrophy Of Corneal Endothelium

Corneal Endothelial Dystrophy 2

Corneal Endothelial Dystrophy 2, Autosomal Recessive, Formerly

Ched2, Formerly

Corneal Endothelial Dystrophy, Autosomal Recessive

Endothelial Dystrophy

Posterior Membrane Corneal Dystrophy

Corneal Endothelial Dystrophy Type 2

Congenital Hereditary Endothelial Dystrophy Of The Cornea

Congenital Hereditary Endothelial Dystrophy Type Ii

Autosomal Recessive Ched

Autosomal Recessive Congenital Hereditary Endothelial Dystrophy

Chedii

Congenital Hereditary Endothelial Dystrophy Type 2

Infantile Hereditary Endothelial Dystrophy

Congenital Hereditary Endothelial Corneal Dystrophy

Corneal Endothelial Dystrophy 2, Autosomal Recessive

Iridocorneal Endothelial Syndrome

Dystrophy, Corneal, Endothelial

Corneal Endothelial Dystrophy 1, Autosomal Dominant

Epithelial And Subepithelial Dystrophy
Recurrent Corneal Erosion

Recurrent Erosion Of Cornea

Recurrent Erosion Syndrome

Corneal Erosion

Non-Traumatic Recurrent Erosion Of Cornea

Corneal Dystrophy, Lisch Epithelial

Lisch Epithelial Corneal Dystrophy

LECD

Band-Shaped And Whorled Microcystic Corneal Epithelial Dystrophy

Band-Shaped And Whorled Microcystic

Band-Shaped And Whorled Microcystic Dystrophy Of The Corneal Epithelium

Corneal Deposit

Deposits - Cornea

Granular Corneal Dystrophy

Granular Dystrophy Corneal

Corneal Dystrophies, Hereditary

Hereditary Corneal Dystrophy

Corneal Dystrophy Nos

Familial Hereditary Corneal Degeneration

Hereditary Corneal Opacity

Hymenolepiasis

Dwarf Tapeworm Infection

Hymenolepis Infectious Disease

Hymenolepsis Infection

Hyemolepis Nana Infection

Hymenolepiosis

Hymenolepis Infection

Dwarf Tapeworm

Hymenolepidosis

Hymenolepis Infestation

Filamentary Keratitis
Corneal Dystrophy, Thiel-Behnke Type

Thiel-Behnke Corneal Dystrophy

Tbcd

CDTB

Cdb2

Corneal Dystrophy Of Bowman Layer Type Ii

Anterior Limiting Membrane Dystrophy Type Ii

Waardenburg-Jonker Corneal Dystrophy

Corneal Dystrophy Of Bowman Layer, Type Ii

Corneal Dystrophy, Honeycomb-Shaped

Corneal Dystrophy Honeycomb-Shaped

Corneal Dystrophy Thiel Behnke Type

Corneal Dystrophy Honeycomb Shaped

Corneal Dystrophy Of The Bowman Layer Type 2

Thiel Behnke Corneal Dystrophy

Anterior Limiting Membrane Dystrophy Type 2

Corneal Dystrophy Of Bowman Layer Type 2

Curly Fiber Corneal Dystrophy

Honeycomb Corneal Dystrophy

Honeycomb-Shaped Corneal Dystrophy

Dystrophy, Corneal, Thiel-Behnke Type

Pseudopterygium
Corneal Dystrophy, Reis-Bucklers Type

Reis-Bucklers Corneal Dystrophy

Rbcd

CDRB

Cdb1

Corneal Dystrophy Of Bowman Layer Type I

Geographic Corneal Dystrophy

Granular Corneal Dystrophy Type Iii

Reis-Bucklers' Corneal Dystrophy

Anterior Limiting Membrane Dystrophy Type I

Corneal Dystrophy Of Bowman Layer Type 1

Corneal Dystrophy Of Bowman Layer, Type I

Corneal Dystrophy, Geographic

Granular Corneal Dystrophy, Type Iii

Corneal Dystrophy Reis Bucklers Type

Corneal Dystrophy Geographic

Reis Bucklers Corneal Dystrophy

Reis Bucklers Dystrophy

Anterior Limiting Membrane Dystrophy Type 1

Atypical Granular Corneal Dystrophy

Granular Corneal Dystrophy Type 3

Superficial Granular Corneal Dystrophy

Corneal Dystrophy Of Bowman Layer, Type 1

Dystrophy, Corneal, Reis-Bucklers Type

Anterior Scleritis
Punctate Epithelial Keratoconjunctivitis

Punctate Keratitis

Thygeson Superficial Punctate Keratitis

Thygeson'S Superficial Punctate Keratitis

Thygeson Superficial Punctate Keratopathy

Punctate Epithelial Keratitis

Keratopathy
Corneal Dystrophy, Avellino Type

Avellino Corneal Dystrophy

CDA

Combined Granular-Lattice Corneal Dystrophy

Cgd2

Granular Corneal Dystrophy Type 2

Acd

Granular Corneal Dystrophy 2

Corneal Dystrophy Avellino Type

Granular Corneal Dystrophy Type Ii

Granular Corneal Dystrophy, Type Ii

Combined Granular-Lattice Corneal Dystrophies

Granular And Lattice Corneal Dystrophies

Granular-Lattice Corneal Dystrophy

Gcd2

Gcdii

Granular-Lattice Corneal Dystrophy

Corneal Dystrophy, Gelatinous Drop-Like

Gelatinous Drop-Like Corneal Dystrophy

GDLD

Cdgdl

Corneal Amyloidosis

Lattice Corneal Dystrophy Type Iii

Amyloidosis, Corneal

Amyloid Corneal Dystrophy, Japanese Type

Gdcd

Primary Familial Amyloidosis Of The Cornea

Subepithelial Amyloidosis Of The Cornea

Corneal Dystrophy, Lattice Type 3

Corneal Dystrophy, Lattice Type Iii

Lattice Corneal Dystrophy, Type Iii

Amyloidosis Corneal

Lattice Corneal Dystrophy Type3

Amyloid Corneal Dystrophy Japanese Type

Dystrophy, Corneal, Gelatinous Drop-Like

Amyloid Of Cornea

Cicatricial Pemphigoid

Mucous Membrane Pemphigoid

Ocular Pemphigoid

Benign Mucous Membrane Pemphigoid

Benign Mucous Membrane Pemphigoid With Ocular Involvement

Benign Mucosal Pemphigoid

Pemphigoid, Benign Mucous Membrane

Cicatricial Pemphigoid With Ocular Involvement

Ocular Pemphigus

Cicatricial Pemphigoid Disease

Mucosal Pemphigoid

Mucosynechial Pemphigoid

Pemphigoid Cicatricial

Cicatricial Pemphigoid Involving The Eye

Ocular Cicatricial Pemphigoid

Macular Dystrophy, Corneal

Macular Corneal Dystrophy

MCD

Corneal Dystrophy, Macular Type

Groenouw Type Ii Corneal Dystrophy

Fehr Corneal Dystrophy

Macular Dystrophy, Corneal Type 1

Mcdc1

Macular Corneal Dystrophy Type Ii

Macular Corneal Dystrophy, Type Ii

Macular Corneal Dystrophy, Type I

Mcdc1, Formerly

Macular Dystrophy, Corneal, 1

Macular Corneal Dystrophy Type 1

Corneal Dystrophy Groenouw Type Ii

Corneal Dystrophy Macular Type

Macular Corneal Dystrophy Type I

Dystrophy, Macular, Corneal

Epithelial Basement Membrane Dystrophy

Ebmd

Corneal Dystrophy, Epithelial Basement Membrane

Cogan Corneal Dystrophy

Microcystic Corneal Dystrophy

Anterior Basement Membrane Dystrophy

Cogan Microcystic Epithelial Dystrophy

Map-Dot-Fingerprint Dystrophy

Microscopic Cystic Corneal Dystrophy

Plica Syndrome

Synovitis

Severe Cutaneous Adverse Reaction

Stevens-Johnson Syndrome

Toxic Epidermal Necrolysis

Drug-Induced Stevens Johnson Syndrome

Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum

Susceptibility To Severe Cutaneous Adverse Reaction

Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

Lyell'S Syndrome

Lyell Syndrome

Severe Cutaneous Adverse Reaction, Susceptibility To

Hypersensitivity Syndrome, Carbamazepine-Induced, Susceptibility To

Hypersensitivity Syndrome, Carbamazepine-Induced

Stevens-Johnson Syndrome, Susceptibility To

Toxic Epidermal Necrolysis, Susceptibility To

Sjs/Ten

Susceptibility To Severe Cutaneous Adverse Reaction Ity To

Mycoplasma-Induced Stevens Johnson Syndrome

Dermatostomatitis, Stevens Johnson Type

Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Spectrum

Sjs-Ten

Toxic Epidermolysis

SJS

Dermatostomatitis Stevens Johnson Type

Ten

Sjs/Ten - [Stevens-Johnson Syndrome And Toxic Epidermal Necrolysis]

Ten - [Toxic Epidermal Necrolysis]

Schnyder Corneal Dystrophy

Schnyder Crystalline Corneal Dystrophy

SCCD

Corneal Dystrophy, Crystalline, Of Schnyder

Corneal Dystrophy, Schnyder Type

Corneal Dystrophy Crystalline Of Schnyder

Crystalline Stromal Dystrophy

Hereditary Crystalline Stromal Dystrophy Of Schnyder

Scd

Corneal Dystrophy, Schnyder

Schnyder Crystalline Dystrophy Sine Crystals

Dystrophy, Corneal, Crystalline, Schnyder

Congenital Disorder Of Glycosylation, Type Iic

CDG2C

Congenital Disorder Of Glycosylation Type Iic

Leukocyte Adhesion Deficiency Type Ii

Cdg Iic

Cdgiic

Rambam-Hasharon Syndrome

Leukocyte Adhesion Deficiency, Type Ii

Lad2

Leukocyte Adhesion Deficiency 2

Cdg-Iic

Congenital Disorder Of Glycosylation, Type 2c

Rhs

Cdg Syndrome Type Iic

Lad-Ii

Rambam Hasharon Syndrome

Congenital Disorder Of Glycosylation 2c

Glycosylation, Congenital Disorder Of, Type Iic

Deep Keratitis
Interstitial Keratitis
Entropion
Epithelial-Stromal Tgfbi Dystrophy
Orbital Granuloma
Corneal Degeneration

Degenerative Corneal Opacity

Corneal Ulcer

Cornea Ulcer

Ulcerative Keratitis

Corneal Ulcer Nos

Aniridia 1

Aniridia

Congenital Aniridia

AN1

An

Cataract With Late-Onset Corneal Dystrophy

Aplasia Of Iris

Absent Iris

Irideremia

Aniridia Ii, Formerly

An2, Formerly

An2

Aniridia Type Ii

Aniridia, Type 1

An-1

Absence Of Iris

Agenesis Of Iris

Congenital Absence Of Iris

Hereditary Aniridia

Sporadic Aniridia

Cardiac Valvular Dysplasia, X-Linked

Xmvd

X-Linked Cardiac Valvular Dysplasia

CVD1

Filamin A-Related X-Linked Myxomatous Valvular Dysplasia

Flna-Related Valvular Dystrophy

Flna-Related X-Linked Myxomatous Valvular Dysplasia

Valvular Heart Disease, Congenital

Myxomatous Valvular Dystrophy, X-Linked

Congenital Valvular Heart Disease

X-Linked Myxomatous Valvular Dystrophy

CVDPX

Ehlers-Danlos Syndrome, Type V, Formerly

Eds5, Formerly

Dystrophie Valvulaire Associee A Flna

Eds 5

Ehlers-Danlos Syndrome, Type 5

Dystrophie Valvulaire Associée À Flna

Filamin-A-Associated Myxomatous Mitral Valve Disease

Filamin-A-Related Myxomatous Mitral Valve Dystrophy

Congenital Valvular Dysplasia

Cvdx

Ehlers-Danlos Syndrome Type 5

Irregular Astigmatism
Corneal Dystrophy, Posterior Polymorphous, 1

Posterior Polymorphous Corneal Dystrophy

Ppcd

Maumenee Corneal Dystrophy

Posterior Polymorphous Corneal Dystrophy 1

PPCD1

Corneal Dystrophy, Hereditary Polymorphous Posterior

Corneal Endothelial Dystrophy 1, Autosomal Dominant

Schlichting Dystrophy

Ched1

Corneal Endothelial Dystrophy 1, Autosomal Dominant, Formerly

Ched1, Formerly

Hereditary Polymorphus Posterior Corneal Dystrophy

Posterior Polymorphous Dystrophy

Hereditary Polymorphous Posterior Corneal Dystrophy

Dystrophy, Corneal, Posterior Polymorphous

Dystrophy, Corneal, Posterior Polymorphous, Type 1

Polymorphous Corneal Dystrophy

Corneal Endothelial Dystrophy 2

Iris Disease

Iris Diseases

Corneal Dystrophy, Subepithelial Mucinous

Subepithelial Mucinous Corneal Dystrophy

SMCD

Corneal Edema

Corneal Oedema

Infiltrate Of Cornea

Meibomian Cyst

Chalazion

Meibomian Gland Lipogranuloma

Tarsal Cyst

Hepatic Infarction

Infarct Of Liver

Hepatic Infarct

Liver Infarct

Liver Infarction

Conjunctival Squamous Cell Carcinoma

Squamous Cell Carcinoma Of Conjunctiva

Conjunctival Epidermoid Carcinoma

Invasive Squamous Cell Carcinoma Of The Conjunctiva

Ocular Surface Squamous Neoplasia

Stromal Dystrophy
Keratitis, Hereditary

Keratitis

Autosomal Dominant Keratitis

Hereditary Keratitis

Dominantly Inherited Keratitis

Keratitis Hereditary

KERH

Keratosis Follicularis Spinulosa Decalvans

Kfsd

Keratosis Follicularis Spinulosa Decalvans Cum Ophiasi

Keratosis Follicularis Spinulosa Decalvans, X-Linked

Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant

Tyrosinemia, Type Ii

Tyrosinemia Type Ii

Oculocutaneous Tyrosinemia

Richner-Hanhart Syndrome

Tyrosine Aminotransferase Deficiency

Tat Deficiency

Tyrosine Transaminase Deficiency

Keratosis Palmoplantaris With Corneal Dystrophy

TYRSN2

Oregon Type Tyrosinemia

Tyrosinemia Type 2

Tyrosinosis Oculocutaneous Type

Tyrosinosis, Oculocutaneous Type

Richner Hanhart Syndrome

Keratosis Palmoplantaris-Corneal Dystrophy Syndrome

Tyrosinemia Due To Tat Deficiency

Tyrosinemia Due To Tyrosine Aminotransferase Deficiency

Tyrosinemia 2

Tyrosinemia Oregon Type

Tyrosine Transaminase Deficiency Disease

Fuchs' Endothelial Dystrophy

Fuchs Endothelial Corneal Dystrophy

Fuchs Endothelial Dystrophy

Fuchs Dystrophy

Fced

Fuchs' Corneal Dystrophy

Fuchs' Endothelial Corneal Dystrophy

Fuchs Atrophy

Fuchs Corneal Dystrophy

Endoepithelial Corneal Dystrophy

Fecd

Late Hereditary Endothelial Dystrophy

Corneal Dystrophy, Fuchs Endothelial

Dystrophy, Corneal, Fuchs Endothelial

Corneal Dystrophy, Fuchs' Endothelial, 1

Breast Disease

Breast Diseases

Eye Disease

Eye Diseases

Abnormality Of The Eye

Toxoplasma Oculopathy

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