| Diseases |
Alias |
|
| Osteoporosis-Pseudoglioma Syndrome |
|
OPPG
|
Ops
|
|
Osteoporosis With Pseudoglioma
|
Osteogenesis Imperfecta, Ocular Form
|
|
Ocular Form Of Osteogenesis Imperfecta
|
Osteogenesis Imperfecta Ocular Form
|
|
Osteoporosis Pseudoglioma Syndrome
|
Pseudoglioma With Bone Fragility
|
|
|
| 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
|
|
|
| Osteopetrosis, Autosomal Dominant 1 |
|
OPTA1
|
Autosomal Dominant Osteopetrosis 1
|
|
Autosomal Dominant Osteopetrosis Type 1
|
Osteopetrosis Autosomal Dominant Type 1
|
|
Osteopetrosis, Autosomal Dominant, Type I
|
Osteopetrosis, Autosomal Dominant, Type 1
|
|
|
| Polycystic Liver Disease 4 With Or Without Kidney Cysts |
|
PCLD4
|
Liver Disease, Polycystic, Type 4, With/Without Kidney Cysts
|
|
|
| Exudative Vitreoretinopathy 4 |
|
EVR4
|
Vitreoretinopathy, Exudative 4
|
|
Vitreoretinopathy, Exudative, Type 4
|
|
|
| Bone Mineral Density Quantitative Trait Locus 1 |
|
BMND1
|
High Bone Mass Trait
|
|
HBM
|
|
|
| Exudative Vitreoretinopathy |
|
Familial Exudative Vitreoretinopathy
|
Fevr
|
|
Criswick-Schepens Syndrome
|
Exudative Vitreoretinopathy, Familial
|
|
Vitreoretinopathy, Exudative )
|
Exudative Vitreoretinopathy 1
|
|
|
| Exudative Vitreoretinopathy 1 |
|
Retinopathy Of Prematurity
|
Retrolental Fibroplasia
|
|
EVR1
|
Criswick-Schepens Syndrome
|
|
Rop
|
Exudative Vitreoretinopathy, Familial, Autosomal Dominant
|
|
Fevr, Autosomal Dominant
|
Premature Retinopathy
|
|
Vitreoretinopathy, Exudative 1
|
Autosomal Dominant Familial Exudative Vitreoretinopathy
|
|
Fevr
|
Vitreoretinopathy, Exudative, Type 1
|
|
Retinopathy Of Prematurity Nos
|
Rlf- [Retrolental Fibroplasia]
|
|
Rop - [Retinopathy Of Prematurity]
|
Terry Syndrome
|
|
|
| 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
|
|
|
| Lrp5-Related Primary Osteoporosis |
|
|
| Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome |
|
|
| Van Buchem Disease |
|
Hyperostosis Corticalis Generalisata
|
Hyperphosphatasemia Tarda
|
|
VBCH
|
Sost-Related Sclerosing Bone Dysplasia
|
|
Endosteal Hyperostosis Autosomal Recessive
|
Sclerosteosis
|
|
Endosteal Hyperostosis, Autosomal Recessive
|
Hyperotosis Corticalis Generalisata Familiaris
|
|
Sost Sclerosing Bone Dysplasia
|
Smith-Lemli-Opitz Syndrome
|
|
|
| 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
|
|
|
| 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
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Vitreoretinopathy |
|
|
| Van Buchem Disease Type 2 |
|
VBCH2
|
Osteosclerosis Of The Skull And Enlarged Mandible
|
|
Van Buchem Disease 2
|
|
|
| Vitreoretinal Degeneration |
|
|
| Osteoporosis, Juvenile |
|
Idiopathic Juvenile Osteoporosis
|
Idiopathic Osteoporosis
|
|
Juvenile Osteoporosis
|
Ijo
|
|
|
| Sclerosteosis |
|
Cortical Hyperostosis With Syndactyly
|
Sost
|
|
Cortical Hyperostosis-Syndactyly Syndrome
|
|
|
| Hyperostosis |
|
Hypertrophy Of Bone
|
Bone Hypertrophy
|
|
Bone Thickening
|
Periosteum Thickening
|
|
|
| Norrie Disease |
|
Atrophia Bulborum Hereditaria
|
Episkopi Blindness
|
|
Pseudoglioma
|
ND
|
|
Norrie-Warburg Disease
|
Anderson-Warburg Syndrome
|
|
Fetal Iritis Syndrome
|
Norrie Syndrome
|
|
Norrie-Warburg Syndrome
|
Ndp
|
|
Congenital Progressive Oculo-Acoustico-Cerebral Degeneration
|
Norrie'S Disease
|
|
Oligophrenia Microphthalmus
|
Pseudoglioma Congenita
|
|
Whitnall-Norman Syndrome
|
|
|
| Osteopetrosis |
|
Marble Bone Disease
|
Albers-Schonberg Disease
|
|
Osteopetroses
|
Marble Bones
|
|
Osteopetrosis And Related Disorders
|
Congenital Osteopetrosis
|
|
Marble Bone
|
Albers-Schoenberg Disease
|
|
Albers-Schonberg Osteopetrosis
|
Osteosclerosis Fragilis
|
|
Ivory Bones
|
|
|
| Retinal Detachment |
|
Retinal Detachments
|
Rhegmatogenous Retinal Detachment
|
|
Ruptured Retina With Detachment
|
Retinal Hole With Detachment
|
|
|
| Camurati-Engelmann Disease |
|
Progressive Diaphyseal Dysplasia
|
Ced
|
|
Engelmann Disease
|
Diaphyseal Dysplasia 1, Progressive
|
|
Pdd
|
Diaphyseal Dysplasia
|
|
Dpd1
|
Camurati-Engelmann Syndrome
|
|
CAEND
|
Engelman'S Disease
|
|
Diaphyseal Hyperostosis
|
Diaphyseal Osteosclerosis
|
|
|
| Mccune-Albright Syndrome |
|
Mass Syndrome
|
Polyostotic Fibrous Dysplasia
|
|
MAS
|
Fibrous Dysplasia Of Bone
|
|
Albright Syndrome
|
Mass Phenotype
|
|
Overlap Connective Tissue Disease
|
Mccune Albright Syndrome
|
|
Osteitis Fibrosa Disseminata
|
OCTD
|
|
Albright'S Disease
|
Pfd
|
|
Pofd
|
Albright'S Syndrome
|
|
Mccune-Albright Syndrome, Somatic, Mosaic
|
Albright'S Disease Of Bone
|
|
Albright'S Syndrome With Precocious Puberty
|
Albright-Mccune-Sternberg Syndrome
|
|
Albright-Sternberg Syndrome
|
Fibrous Dysplasia With Pigmentary Skin Changes And Precocious Puberty
|
|
Gonadotropin-Independent Female-Limited Sexual Precocity
|
Fibrous Dysplasia Polyostotic
|
|
Fibrous Dysplasia, Polyostotic
|
|
|
| Type 1 Diabetes Mellitus |
|
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
|
IDDM
|
Type 1 Diabetes
|
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
|
Juvenile-Onset Diabetes
|
Jod
|
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
|
Diabetes Type 1
|
Type I Diabetes
|
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
| Osteonecrosis |
|
Bone Necrosis
|
Avascular Necrosis Of Bone
|
|
Aseptic Necrosis
|
Necrosis Of Bone Nos
|
|
Aseptic Osteonecrosis
|
Aseptic Necrosis Of Bone, Site Unspecified
|
|
Aseptic Or Avascular Bone Necrosis
|
Aseptic Necrosis Of Bone
|
|
Necrotic Bone
|
Necrotizing Bone
|
|
Spontaneous Osteonecrosis
|
Osteoradionecrosis
|
|
|
| Craniodiaphyseal Dysplasia |
|
CDD
|
Schaefer Stein Oshman Syndrome
|
|
Craniodiaphyseal Dysplasia, Dominant
|
Dominantly Inherited Craniodiaphyseal Dysplasia
|
|
|
| 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]
|
|
|
| Type 1 Diabetes Mellitus 4 |
|
Diabetes Mellitus, Insulin-Dependent, 4
|
Iddm4
|
|
Insulin-Dependent Diabetes Mellitus 4
|
T1D4
|
|
Insulin-Dependent Diabetes Mellitus-4
|
|
|
| Craniodiaphyseal Dysplasia, Autosomal Dominant |
|
CDD
|
Autosomal Dominant Craniodiaphyseal Dysplasia
|
|
Schaefer Stein Oshman Syndrome
|
Craniodiaphyseal Dysplasia Autosomal Dominant
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Diabetes Mellitus |
|
|
| Hypotrichosis Simplex |
|
Hereditary Hypotrichosis Simplex
|
Hhs
|
|
|
| Craniosynostosis |
|
Premature Closure Of Cranial Sutures
|
Craniostenosis
|
|
Craniosynostosis Syndrome
|
Cso
|
|
Craniosynostoses
|
Congenital Ossification Of Cranial Sutures
|
|
Congenital Ossification Of Sutures Of Skull
|
Craniostosis
|
|
Imperfect Fusion Of Skull
|
Congenital Imperfect Closure Skull
|
|
Imperfect Closure Skull
|
Premature Closure Cranium Sutures
|
|
Deficiency Of Craniofacial Axis
|
|
|
| Sclerosteosis 2 |
|
SOST2
|
Sclerosteosis, Type 2
|
|
|
| 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
|
|
|
| Bone Disease |
|
Bone Diseases
|
Skeletal Disease
|
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
| Ectodermal Dysplasia 13, Hair/Tooth Type |
|
ECTD13
|
Ectodermal Dysplasia 13
|
|
|
| Hypotrichosis |
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Osteopetrosis, Autosomal Dominant 2 |
|
OPTA2
|
Autosomal Dominant Osteopetrosis 2
|
|
Osteopetrosis Autosomal Dominant Type 2
|
Osteopetrosis, Autosomal Dominant, Type Ii
|
|
Albers-Schonberg Osteopetrosis
|
Autosomal Dominant Albers-Schonberg Disease
|
|
Osteopetrosis
|
Marble Bones, Autosomal Dominant
|
|
Osteosclerosis Fragilis Generalisata
|
Albers-Schonberg Disease, Autosomal Dominant
|
|
Autosomal Dominant Osteopetrosis Type Ii
|
Albers-Schönberg Osteopetrosis
|
|
Autosomal Dominant Osteopetrosis Type 2
|
Marble Disease Autosomal Dominant
|
|
Osteopetrosis, Autosomal Dominant, Type 2
|
|
|
| Glucocorticoid-Induced Osteoporosis |
|
Steroid-Induced Osteoporosis
|
|
|
| Bone Resorption Disease |
|
|
| Slate Pneumoconiosis |
|
|
| Bone Remodeling Disease |
|
|
| Osteogenesis Imperfecta, Type Xv |
|
Osteogenesis Imperfecta Type 15
|
OI15
|
|
Osteogenesis Imperfecta Type Xv
|
Oi, Type Xv
|
|
Osteogenesis Imperfecta 15
|
Oi Type Xv
|
|
Oi-Xv
|
|
|
| Digeorge Syndrome |
|
Chromosome 22q11.2 Deletion Syndrome
|
DGS
|
|
Hypoplasia Of Thymus And Parathyroids
|
Third And Fourth Pharyngeal Pouch Syndrome
|
|
22q11.2 Deletion Syndrome
|
Digeorge Sequence
|
|
Digeorge'S Syndrome
|
Pharyngeal Pouch Syndrome
|
|
Di-George Syndrome
|
Shprintzen Syndrome
|
|
|
| Persistent Hyperplastic Primary Vitreous |
|
Congenital Retinal Detachment
|
Ncrna Disease
|
|
Non-Syndromic Congenital Retinal Non-Attachment
|
Pfvs
|
|
Phpv
|
Persistent Fetal Vasculature Syndrome
|
|
|
| Leukocoria |
|
|
| Osteopathia Striata With Cranial Sclerosis |
|
Hyperostosis Generalisata With Striations
|
Robinow-Unger Syndrome
|
|
OSCS
|
Osteopathia Striata Cranial Sclerosis
|
|
Osteopathia Striata-Cranial Sclerosis Syndrome
|
Horan-Beighton Syndrome
|
|
Os-Cs
|
Osteopathia Striata - Cranial Sclerosis
|
|
Voorhoeve Disease
|
Osc
|
|
|
| Cenani-Lenz Syndactyly Syndrome |
|
Syndactyly Type 7
|
Cenani Syndactylism
|
|
Cenani-Lenz Syndactyly
|
CLSS
|
|
Syndactyly Cenani Lenz Type
|
Cenani-Lenz Syndrome
|
|
Syndactyly, Type Vii
|
Cenani-Lenz Type Syndactyly
|
|
Cenani Syndactyly
|
Syndactyly Type Vii
|
|
|
| Retinal Telangiectasia |
|
|
| Dilated Cardiomyopathy 1t |
|
Cmd1t
|
Cardiomyopathy, Dilated, 1t
|
|
|
| Coats Disease |
|
Exudative Retinopathy
|
Retinal Telangiectasis
|
|
Coats' Disease
|
Leber Miliary Aneurysm
|
|
Coats' Syndrome
|
Congenital Retinal Telangiectasia
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Focal Segmental Glomerulosclerosis |
|
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
|
Focal Glomerulosclerosis
|
|
Fsgs
|
Segmental Glomerulosclerosis
|
|
Glomerulosclerosis, Focal Segmental
|
Fgs
|
|
Focal Glomerular Sclerosis
|
Familial Idiopathic Nephrotic Syndrome
|
|
Focal Sclerosis With Hyalinosis
|
Glomerulosclerosis, Focal
|
|
Glomerulosclerosis Focal
|
Glomerulosclerosis, Segmental, Focal
|
|
Focal Segmental Glomerulosclerosis, Not Otherwise Specified
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Zygodactyly
|
|
Syndactyly, Type I
|
Sd1
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Symphalangism
|
|
Non-Syndromic Syndactyly
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Tetraamelia Syndrome |
|
Tetra-Amelia Syndrome
|
Tetraamelia-Multiple Malformations Syndrome
|
|
Tetra-Amelia
|
Tetra-Amelia, Autosomal Recessive
|
|
Tetraamelia, Autosomal Recessive
|
Total Amelia
|
|
Zimmer Phocomelia
|
Tetams
|
|
Zimmer Taub Sova Syndrome
|
|
|
| Robinow Syndrome |
|
Acral Dysostosis With Facial And Genital Abnormalities
|
Fetal Face Syndrome
|
|
Robinow Dwarfism
|
Mesomelic Dwarfism-Small Genitalia Syndrome
|
|
Robinow-Silverman-Smith Syndrome
|
Costovertebral Segmentation Defect With Mesomelia
|
|
Covesdem Syndrome
|
Robinow'S Syndrome
|
|
Robinow-Silverman Syndrome
|
|
|
| Retinitis Pigmentosa 7 |
|
Leber Congenital Amaurosis 18
|
RP7
|
|
Retinitis Pigmentosa 7, Digenic Form
|
Retinitis Pigmentosa 7 And Digenic Form
|
|
Retinitis Pigmentosa 7, Digenic
|
LCA18
|
|
Retinitis Pigmentosa 7 Digenic
|
|
|
| Bone Development Disease |
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Aortic Valve Disease 1 |
|
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
|
Aortic Valve Disorder
|
AOVD1
|
|
Bav
|
Bicuspid Aortic Valve Disease
|
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
|
Aovd
|
Aortic Valve, Bicuspid
|
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
|
Familial Bav
|
Calcific Aortic Stenosis
|
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
|
Bicommissural Aortic Valve
|
|
|
| Tooth Agenesis |
|
Oligodontia
|
Hypodontia
|
|
Selective Tooth Agenesis
|
Tooth Agenesis, Selective
|
|
Familial Tooth Agenesis
|
Anodontia
|
|
Congenital Absence Of One Tooth
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
