| Diseases |
Alias |
|
| Osteogenesis Imperfecta, Type Iii |
|
Osteogenesis Imperfecta Type Iii
|
OI3
|
|
Oi, Type Iii
|
Osteogenesis Imperfecta Type 3
|
|
Oi Type Iii
|
Oi Type 3
|
|
Progressive Deforming Osteogenesis Imperfecta
|
Severe Osteogenesis Imperfecta
|
|
Osteogenesis Imperfecta, Progressively Deforming, With Normal Sclerae
|
Progressively Deforming Osteogenesis Imperfecta With Normal Sclera
|
|
Osteogenesis Imperfecta, Progressively Deforming With Normal Sclerae
|
Progressively Deforming Oi
|
|
Osteogenesis Imperfecta 3
|
Oi-Iii
|
|
Progressively Deforming Osteogenesis Imperfecta With Normal Sclerae
|
|
|
| Osteogenesis Imperfecta, Type Iv |
|
Osteogenesis Imperfecta Type 4
|
Osteogenesis Imperfecta Type Iv
|
|
OI4
|
Oi, Type Iv
|
|
Osteogenesis Imperfecta With Normal Sclerae
|
Oi Type Iv
|
|
Oi Type 4
|
Osteogenesis Imperfecta With Normal Sclera
|
|
Common Variable Oi With Normal Sclerae
|
Osteogenesis Imperfecta 4
|
|
Oi-Iv
|
|
|
| Osteogenesis Imperfecta, Type Ii |
|
Vrolik Type Of Osteogenesis Imperfecta
|
Osteogenesis Imperfecta Type 2
|
|
OI2
|
Oi, Type Ii
|
|
Osteogenesis Imperfecta Congenita
|
Oic
|
|
Osteogenesis Imperfecta Type Ii
|
Lethal Osteogenesis Imperfecta
|
|
Oi Type 2
|
Osteogenesis Imperfecta Congenita Perinatal Lethal Form
|
|
Osteogenesis Imperfecta Congenita, Perinatal Lethal Form
|
Perinatal Lethal Osteogenesis Imperfecta Congenita
|
|
Perinatally Lethal Oi
|
Osteogenesis Imperfecta 2
|
|
Oi-Ii
|
Oi-Iia
|
|
Oi Type Iia
|
Osteogenesis Imperfecta Type Iia
|
|
Osteogenesis Imperfecta Type Ii Autosomal Dominant
|
Oi Type Ii
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
|
|
| Ehlers-Danlos Syndrome, Cardiac Valvular Type |
|
EDSCV
|
Cardiac-Valvular Ehlers-Danlos Syndrome
|
|
Cardiac-Valvular Eds
|
Ehlers-Danlos Syndrome, Autosomal Recessive, Cardiac Valvular Form
|
|
Cveds
|
Ehlers-Danlos Syndrome Cardiac Valvular Type
|
|
Eds, Cardiac Valvular Type
|
|
|
| Combined Osteogenesis Imperfecta And Ehlers-Danlos Syndrome 2 |
|
|
| Ehlers-Danlos Syndrome, Arthrochalasia Type, 2 |
|
Eds Viib
|
EDSARTH2
|
|
Ehlers-Danlos Syndrome, Type Viib, Autosomal Dominant
|
Eds7b
|
|
Ehlers-Danlos Syndrome Arthrochalasia Type 2
|
Ehlers-Danlos Syndrome Type 7b
|
|
Ehlers-Danlos Syndrome 7b
|
Ehlers-Danlos Syndrome, Arthrochalasia, Type 2
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Osteogenesis Imperfecta, Type I |
|
Osteogenesis Imperfecta Type I
|
OI1
|
|
Oi, Type I
|
Osteogenesis Imperfecta Tarda
|
|
Osteogenesis Imperfecta With Blue Sclerae
|
Osteogenesis Imperfecta Type 1
|
|
Adair-Dighton Syndrome
|
Mild Osteogenesis Imperfecta
|
|
Non-Deforming Osteogenesis Imperfecta
|
Oi Type 1
|
|
Van Der Hoeve Syndrome
|
Classic Non-Deforming Oi With Blue Sclerae
|
|
Osteogenesis Imperfecta 1
|
Oi-I
|
|
Osteopenic Non-Fracture Syndrome
|
Osteogenesis Imperfecta, Mild
|
|
Osteogenesis Imperfecta
|
Lobstein'S Disease
|
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
| Dentinogenesis Imperfecta |
|
Hereditary Opalescent Dentin
|
Dentinogenesis Imperfecta Without Osteogenesis Imperfecta
|
|
Dgi
|
Capdepont Teeth
|
|
Dgi Without Oi
|
Di
|
|
Non-Syndromic Dgi
|
Non-Syndromic Dentinogenesis Imperfecta
|
|
Opalescent Teeth Without Oi
|
Opalescent Teeth Without Osteogenesis Imperfecta
|
|
Opalescent Dentin
|
|
|
| Ehlers-Danlos Syndrome, Classic Type, 1 |
|
Ehlers-Danlos Syndrome, Type I
|
EDSCL1
|
|
Ehlers-Danlos Syndrome Classic Type 1
|
Ehlers-Danlos Syndrome Type 1
|
|
Ehlers-Danlos Syndrome, Type I, Formerly
|
Eds1, Formerly
|
|
Ehlers-Danlos Syndrome, Severe Classic Type, Formerly
|
Eds I, Formerly
|
|
Ehlers-Danlos Syndrome, Gravis Type, Formerly
|
Ehlers-Danlos Syndrome, Type 1
|
|
Type I Ehlers-Danlos Syndrome
|
Eds1
|
|
Eds I
|
Ehlers-Danlos Syndrome, Gravis Type
|
|
Ehlers-Danlos Syndrome, Severe Classic Type
|
Ehlers-Danlos Syndrome 1
|
|
Ehlers-Danlos, Classic Syndrome, Type 1
|
Ehlers-Danlos Syndrome Type 2
|
|
|
| Ehlers-Danlos/Osteogenesis Imperfecta Syndrome |
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Ehlers-Danlos Syndrome, Arthrochalasia Type, 1 |
|
Arthrochalasis Multiplex Congenita
|
Eds7a
|
|
Ehlers-Danlos Syndrome Type 7a
|
Ehlers-Danlos Syndrome, Arthrochalasia Type
|
|
EDSARTH1
|
Eds Viia
|
|
Eds Vii, Mutant Procollagen Type
|
Arthrochalasia Ehlers-Danlos Syndrome
|
|
Arthrochalasia Eds
|
Aeds
|
|
Ehlers-Danlos Syndrome, Type Viia
|
Ehlers-Danlos Syndrome, Type Viia, Autosomal Dominant
|
|
Ehlers-Danlos Syndrome Arthrochalasia Type 1
|
Eds Vii
|
|
Ehlers-Danlos Syndrome Type 7
|
Eds Vii Mutant Procollagen Type
|
|
Ehlers-Danlos Syndrome 7a
|
Ehlers-Danlos Syndrome Arthrochalasic Type
|
|
Ehlers-Danlos Syndrome Type Viia, Autosomal Dominant
|
Eds Viib
|
|
|
| Classic Ehlers-Danlos Syndrome |
|
Ehlers-Danlos Syndrome, Classic Type
|
Classical Ehlers-Danlos Syndrome
|
|
Eds, Classic Type
|
Ehlers-Danlos Syndrome Type 1
|
|
Ehlers-Danlos Syndrome Type 2
|
Classical Eds
|
|
Ceds
|
Ehlers-Danlos Syndrome, Type 2
|
|
|
| High Bone Mass Osteogenesis Imperfecta |
|
|
| Primary Bone Dysplasia |
|
Primary Osteodysplasia
|
Primary Skeletal Dysplasia
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Otosclerosis |
|
|
| X-Linked Alport Syndrome |
|
Nephropathy And Deafness, X-Linked
|
|
|
| Idiopathic Scoliosis |
|
|
| Bone Development Disease |
|
|
| Scoliosis |
|
|
| Chiari Malformation |
|
|
| Scirrhous Adenocarcinoma |
|
Adenocarcinoma, Scirrhous
|
Adenocarcinoma With Productive Fibrosis
|
|
|
| Spinal Stenosis |
|
Lumbar Spinal Stenosis
|
Cervical Spinal Stenosis
|
|
Spinal Stenosis Of Lumbar Region
|
Spinal Stenosis In Cervical Region
|
|
Spinal Canal Stenosis
|
|
|
| Alport Syndrome |
|
Hereditary Nephritis
|
Alport Syndrome, X-Linked
|
|
Hemorrhagic Hereditary Nephritis
|
Congenital Hereditary Hematuria
|
|
Hemorrhagic Familial Nephritis
|
Familial Nephritis
|
|
Thin Basement Membrane Disease
|
Thin Basement Membrane Nephropathy
|
|
Hematuria-Nephropathy-Deafness Syndrome
|
Hematuric Hereditary Nephritis
|
|
Hereditary Familial Congenital Hemorrhagic Nephritis
|
Hereditary Hematuria Syndrome
|
|
Hereditary Interstitial Pyelonephritis
|
Alport Deafness-Nephropathy
|
|
Alport Hearing Loss-Nephropathy
|
Alports Syndrome
|
|
Nephritis, Hereditary
|
|
|
| Caffey Disease |
|
Infantile Cortical Hyperostosis
|
CAFYD
|
|
Cortical Congenital Hyperostosis
|
Caffey-Silverman Syndrome
|
|
De Toni-Caffey Disease
|
Hyperostosis Cortical Infantile
|
|
Hyperostosis, Cortical, Congenital
|
|
|
| Oral Submucous Fibrosis |
|
Oral Submucosal Fibrosis, Including Of Tongue
|
Osmf
|
|
Oral Cavity Submucous Fibrosis
|
Oral Submucosal Fibrosis
|
|
Submucosal Fibrosis
|
|
|
| Pelvic Organ Prolapse |
|
Rectal Prolapse
|
Pelvic Organ Prolapse, Susceptibility To, 1
|
|
Pelvic Organ Prolapse, Susceptibility To
|
Prolapse Of Vagina And Rectum
|
|
Vaginal Prolapse
|
Pelvic Organ Prolapse 1
|
|
Procidentia, Rectum
|
Prolapse Of Rectal Mucosa
|
|
Procidentia Of Rectum
|
Rectal Mucosa Prolapse
|
|
Rectum Prolapse
|
Procidentia Rectum
|
|
Rp - [Rectal Prolapse]
|
Male Proctocele
|
|
Male Rectocele
|
Proctoptosis
|
|
Female Genital Prolapse
|
Female Prolapse
|
|
Incompetence Of Pelvic Fundus
|
Relaxation Of Perineum
|
|
Deficiency Of Perineum
|
|
|
| Breast Scirrhous Carcinoma |
|
Infiltrating Carcinoma Of Breast With Fibrotic Stroma
|
Scirrhous Carcinoma Of Breast
|
|
|
| Bruck Syndrome |
|
Osteogenesis Imperfecta With Congenital Joint Contractures
|
Osteogenesis Imperfecta-Congenital Joint Contractures Syndrome
|
|
|
| Systemic Scleroderma |
|
Scleroderma
|
Progressive Systemic Sclerosis
|
|
Systemic Sclerosis
|
Scleroderma, Systemic
|
|
Scleroderma Syndrome
|
Dermatosclerosis
|
|
Familial Progressive Scleroderma
|
Progressive Scleroderma
|
|
Scleroderma Disease
|
Scleroderma, Localized
|
|
Diffuse Scleroderma
|
Scleroderma, Familial Progressive
|
|
|
| Scleroderma, Familial Progressive |
|
Systemic Sclerosis
|
Systemic Scleroderma
|
|
Systemic Sclerosis, Susceptibility To
|
Sclerosis Systemic
|
|
Crest Syndrome
|
Progressive Scleroderma
|
|
|
| Osteogenesis Imperfecta, Type Xiv |
|
Osteogenesis Imperfecta Type 14
|
OI14
|
|
Osteogenesis Imperfecta Type Xiv
|
Oi, Type Xiv
|
|
Osteogenesis Imperfecta 14
|
Oi Type Xiv
|
|
Oi-Xiv
|
|
|
| Pulmonary Fibrosis |
|
|
| Syndromic X-Linked Intellectual Disability Cabezas Type |
|
Cabezas Syndrome
|
Syndromic X-Linked Mental Retardation 15
|
|
Mental Retardation, X-Linked, Syndromic 15
|
Mrss
|
|
Mrxs15
|
Mrxsc
|
|
X-Linked Mental Retardation With Short Stature
|
X-Linked Mental Retardation With Short Stature, Hypogonadism, And Abnormal Gait
|
|
Mental Retardation, X-Linked, With Short Stature
|
Mental Retardation, X-Linked, With Short Stature, Hypogonadism, And Abnormal Gait
|
|
|
| Fibrogenesis Imperfecta Ossium |
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| Osteogenesis Imperfecta, Type V |
|
Osteogenesis Imperfecta Type 5
|
OI5
|
|
Osteogenesis Imperfecta Type V
|
Oi Type 5
|
|
Oi Type V
|
Oi, Type V
|
|
Oi With Calcification In Interosseous Membranes
|
Type V Oi
|
|
Osteogenesis Imperfecta 5
|
Oi-V
|
|
|
| Spondyloepimetaphyseal Dysplasia, Strudwick Type |
|
Spondylometaphyseal Dysplasia
|
Strudwick Syndrome
|
|
Dappled Metaphysis Syndrome
|
Semd, Strudwick Type
|
|
Spondylometaepiphyseal Dysplasia Congenita, Strudwick Type
|
Smed, Strudwick Type
|
|
Smd
|
Smed Strudwick Type
|
|
SEMDSTWK
|
Smed, Type I
|
|
Semdc
|
Smed Type 1
|
|
Spondyloepimetaphyseal Dysplasia Strudwick Type
|
Sed Strudwick
|
|
Spondyloepimetaphyseal Dysplasia Congenita, Strudwick Type
|
Smed Type I
|
|
Spondyloepiphyseal Dysplasia Congenita With Dappled Metaphyses
|
Dysplasia, Spondyloepimetaphyseal, Strudwick Type
|
|
Dysplasia, Spondylometaphyseal
|
|
|
| Osteogenesis Imperfecta, Type Vi |
|
OI6
|
Osteogenesis Imperfecta Type 6
|
|
Osteogenesis Imperfecta Type Vi
|
Oi Type Vi
|
|
Oi Type 6
|
Osteogenesis Imperfecta Type
|
|
Serpinfi- Related Osteogenesis Imperfecta
|
Osteogenesis Imperfecta 6
|
|
Oi-Vi
|
|
|
| Endosteal Hyperostosis, Autosomal Dominant |
|
Osteosclerosis
|
Worth Syndrome
|
|
Osteosclerosis, Autosomal Dominant
|
Hyperostosis, Endosteal
|
|
Endosteal Hyperostosis, Worth Type
|
Worth Disease
|
|
Autosomal Dominant Endosteal Hyperostosis
|
Autosomal Dominant Osteosclerosis, Worth Type
|
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus
|
Autosomal Dominant Osteosclerosis
|
|
Benign Form Of Worth Hyperostosis Corticalis Generalisata With Torus Platinus
|
Worth'S Syndrome
|
|
Worth Type Autosomal Dominant Osteosclerosis
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis, Autosomal Dominant, Worth Type
|
WENHY
|
|
Endosteal Hyperostosis Autosomal Dominant
|
Hyperostosis Corticalis Generalisata Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis Autosomal Dominant
|
Acquired Osteosclerosis
|
|
|
| Stickler Syndrome |
|
Arthroophthalmopathy
|
Hereditary Arthro-Ophthalmo-Dystrophy
|
|
Hereditary Arthro-Ophthalmopathy
|
Stickler Dysplasia
|
|
Hereditary Progressive Arthroophthalmopathy
|
Stickler Syndrome, Type 1
|
|
|
| Collagen Disease |
|
Collagen Diseases
|
Collagen Disorder
|
|
|
| Osteoporosis, Juvenile |
|
Idiopathic Juvenile Osteoporosis
|
Idiopathic Osteoporosis
|
|
Juvenile Osteoporosis
|
Ijo
|
|
|
| Localized Scleroderma |
|
Morphea
|
Localised Scleroderma
|
|
Localized Fibrosing Scleroderma
|
Circumscribed Scleroderma
|
|
Localised Morphea
|
Localised Morphoea
|
|
Localized Morphea
|
Scleroderma, Circumscribed Or Localised
|
|
Scleroderma, Circumscribed Or Localized
|
Scleroderma, Localized
|
|
|
| Dentin Dysplasia |
|
Dentinal Dysplasia
|
Dd
|
|
Dysplasia, Dentin
|
Shell Teeth
|
|
|
| Dental Fluorosis |
|
Mottled Teeth
|
Intrinsic Enamel Discolouration Of Fluorosis
|
|
Mottling Of Enamel
|
Fluorosis, Dental
|
|
Dental Fluorosis, Acquired
|
|
|
| Hypophosphatasia, Adult |
|
Adult Hypophosphatasia
|
Odontohypophosphatasia
|
|
Hypophosphatasia, Mild
|
HPPA
|
|
Hypophosphatasia
|
Mild Hypophosphatasia
|
|
Adult Rathbun Disease
|
Adult Phosphoethanolaminuria
|
|
HOPS
|
|
|
| Cole-Carpenter Syndrome |
|
Cole Carpenter Syndrome
|
Bone Fragility Craniosynostosis Proptosis Hydrocephalus
|
|
Bone Fragility With Craniosynostosis, Ocular Proptosis, Hydrocephalus, And Distinctive Facial Features
|
Bone Fragility-Craniosynostosis-Proptosis-Hydrocephalus Syndrome
|
|
|
| Hypermobility Syndrome |
|
Benign Joint Hypermobility
|
|
|
| Scheuermann Disease |
|
Scheuermann'S Disease
|
Spinal Osteochondrosis
|
|
Juvenile Osteochondrosis Of Spine
|
Familial Scheuermann Disease
|
|
Familial Scheuermann Juvenile Kyphosis
|
Familial Spinal Osteochondrosis
|
|
Scheuermann Juvenile Kyphosis
|
Juvenile Osteochondritis Of The Spine
|
|
Juvenile Osteochondrosis Of Scheurermann
|
Scheuermann'S Kyphosis
|
|
Sherman'S Disease
|
Juvenile Kyphosis
|
|
Scheuermann Kyphosis
|
[X]Spinal Osteochondrosis, Unspecified
|
|
|
| Beach Ear |
|
Acute Swimmer'S Ear
|
Acute Bacterial Inflammation Of External Ear
|
|
Acute Otitis Externa, Diffuse
|
Acute Swimmers' Ear
|
|
Tank Ear
|
|
|
| Bone Structure Disease |
|
|
| Amebiasis |
|
Amoebiasis
|
Entamoebiasis
|
|
Chronic Intestinal Amebiasis
|
Amoebiasis, Unspecified
|
|
Amebic Colitis
|
Amoebic Enteritis
|
|
Infection Due To Entamoeba Histolytica
|
Amoebic Infection
|
|
Disease Due To Endamoebidae
|
Amoebiasis Nos
|
|
|
| Achondrogenesis |
|
|
| Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive |
|
Split Hand-Foot Malformation 1 With Sensorineural Hearing Loss
|
SHFM1D
|
|
Deafness, Congenital, With Split Hands And Feet
|
Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss
|
|
Congenital Deafness With Split Hands And Feet
|
Split Hand-Split Foot-Deafness Syndrome
|
|
Split Hand-Split Foot-Hearing Loss Syndrome
|
Congenital Deafness And Split Hands And Feet
|
|
Split-Hand/Foot Malformation, Type 1 With Sensorineural Hearing Loss
|
Split-Hand-Foot Malformation With Sensorineural Hearing Loss
|
|
|
| Osteogenesis Imperfecta, Type Xi |
|
Osteogenesis Imperfecta Type 11
|
OI11
|
|
Osteogenesis Imperfecta Type Xi
|
Oi, Type Xi
|
|
Osteogenesis Imperfecta 11
|
Oi Type Xi
|
|
Oi-Xi
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Bone Remodeling Disease |
|
|
| Bone Resorption Disease |
|
|
| Loeys-Dietz Syndrome |
|
Loeys-Dietz Aortic Aneurysm Syndrome
|
Lds
|
|
Aortic Aneurysm Syndrome Due To Tgf-Beta Receptors Anomalies
|
Furlong Syndrome
|
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Gastric Carcinoma
|
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Orthostatic Intolerance |
|
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
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Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
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Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
|
OI
|
Intolerance, Orthostatic
|
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
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Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
| Distal Arthrogryposis |
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis
|
|
Congenital Multiple Arthrogryposis
|
Congenital Arthromyodysplasia
|
|
Fibrous Ankylosis Of Multiple Joints
|
Guerin-Stern Syndrome
|
|
Guérin-Stern Syndrome
|
Myodystrophia Fetalis Deformans
|
|
Otto Syndrome
|
Rocher-Sheldon Syndrome
|
|
Rossi Syndrome
|
Amc
|
|
Multiple Congenital Arthrogryposis
|
Arthrogryposis Syndrome
|
|
Arthrogryposis, Distal
|
Distal Arthrogryposis Syndrome
|
|
Freeman-Sheldon Syndrome
|
Arthrogryposis, Distal, Type 2b
|
|
Congenital Multiplex Arthrogryposis
|
Amyoplasia Congenita
|
|
Congenital Amyoplasia
|
Amc - [Arthrogryposis Multiplex Congenita]
|
|
|
| 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
|
|
|
| Tooth Agenesis |
|
Oligodontia
|
Hypodontia
|
|
Selective Tooth Agenesis
|
Tooth Agenesis, Selective
|
|
Familial Tooth Agenesis
|
Anodontia
|
|
Congenital Absence Of One Tooth
|
|
|
| Limited Scleroderma |
|
Limited Cutaneous Systemic Sclerosis
|
Limited Systemic Sclerosis
|
|
Systemic Sclerosis Sine Scleroderma
|
Crest Syndrome
|
|
Limited Cutaneous Systemic Scleroderma
|
Scleroderma, Limited
|
|
Systemic Sclerosis, Limited
|
Progressive Systemic Sclerosis Sine Scleroderma
|
|
Scleroderma, Sine
|
Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome
|
|
Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome
|
|
|
| Interstitial Lung Disease 2 |
|
Idiopathic Pulmonary Fibrosis
|
Ipf
|
|
Fibrocystic Pulmonary Dysplasia
|
Pulmonary Fibrosis, Idiopathic
|
|
Pulmonary Fibrosis, Idiopathic, Susceptibility To
|
Cryptogenic Fibrosing Alveolitis
|
|
ILD2
|
Idiopathic Pulmonary Fibrosis, Familial
|
|
Fibrosing Alveolitis, Cryptogenic
|
Uip
|
|
Fibrosing Alveolitis
|
Interstitial Pneumonitis, Usual
|
|
Familial Idiopathic Pulmonary Fibrosis
|
Idiopathic Fibrosing Alveolitis, Chronic Form
|
|
Usual Interstitial Pneumonia
|
Fibrosing Alveolitis Cryptogenic
|
|
Hamman-Rich Disease
|
Idiopathic Pulmonary Fibrosis Familial
|
|
Interstitial Pneumonitis Usual
|
Fibrosis Idiopathic Pulmonary
|
|
Fibrosis, Pulmonary, Idiopathic
|
Hamman-Rich Syndrome
|
|
Chronic Idiopathic Pulmonary Fibrosis
|
Acute Interstitial Pneumonia
|
|
Interstitial Pulmonary Fibrosis
|
Ipf - [Idiopathic Pulmonary Fibrosis]
|
|
Idiopathic Lung Fibrosis
|
Fibrosing Lung Disease
|
|
Pulmonary Fibrosis Nos
|
Fibrosing Pneumonitis
|
|
|
| Aortic Aneurysm, Familial Thoracic 1 |
|
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
|
AAT1
|
Faa1
|
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
|
Aneurysm, Thoracic Aortic
|
Faa
|
|
Ftaad
|
Taa
|
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
|
Dissection Of Thoracic Aorta
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
