疾病名称 |
别名 |
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Alport Syndrome 1, X-Linked |
Nephropathy And Deafness, X-Linked
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ATS1
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Ats
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Nephritis-Deafness Syndrome, X-Linked
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X-Linked Alport Syndrome |
Nephropathy And Deafness, X-Linked
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Alport Syndrome |
Hereditary Nephritis
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Alport Syndrome, X-Linked
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Hemorrhagic Hereditary Nephritis
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Congenital Hereditary Hematuria
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Hemorrhagic Familial Nephritis
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Familial Nephritis
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Thin Basement Membrane Disease
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Thin Basement Membrane Nephropathy
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Hematuria-Nephropathy-Deafness Syndrome
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Hematuric Hereditary Nephritis
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Hereditary Familial Congenital Hemorrhagic Nephritis
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Hereditary Hematuria Syndrome
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Hereditary Interstitial Pyelonephritis
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Alport Deafness-Nephropathy
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Alport Hearing Loss-Nephropathy
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Alports Syndrome
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Nephritis, Hereditary
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Autosomal Dominant Alport Syndrome |
Alport Syndrome, Autosomal Dominant
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Alport Syndrome Dominant Type
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Renal Failure And Sensorineural Hearing Loss
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Alport Syndrome, Dominant Type
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Alport Syndrome 3, Autosomal Dominant |
ATS3
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Nephritis-Deafness Syndrome
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Nephropathy And Deafness
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Chronic Kidney Disease |
Chronic Renal Disease
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Chronic Kidney Failure
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Ckd
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Chronic Renal Failure
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Kidney Failure, Chronic
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Chronic Renal Failure Syndrome
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Crf
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Renal Failure - Chronic
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Renal Failure Chronic
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Chronic Kidney Diseases
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Chronic Kidney Disease Stage 5
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Ckd - [Chronic Kidney Disease]
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Crf - [Chronic Renal Failure]
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Chronic Kidney Impairment
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Chronic Renal Impairment
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Chronic Kidney Shutdown
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Chronic Hypoxic Kidney Failure
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Chronic Kidney Collapse
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Chronic Renal Insufficiency
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Chronic Kidney Toxaemia
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Chronic Kidney Hypofunction
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Chronic Renal Suppression
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Chronic Renal Failure, Stage 5
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Ckd - [Chronic Kidney Disease] Stage 5
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End Stage Kidney Failure
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End Stage Renal Failure
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End Stage Kidney Disease
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End Stage Renal Disease
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End Stage Chronic Renal Failure
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Esrf - [End Stage Renal Failure]
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Esrd - [End Stage Renal Diseases]
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Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
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Nephrotic Syndrome |
Finnish Congenital Nephrotic Syndrome
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Ns - [Nephrotic Syndrome]
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Nephrosis Syndrome
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Nephrosis Nos
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Glomerular Lesion Nephrosis
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Isolated Macular Dystrophy |
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Focal Segmental Glomerulosclerosis |
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
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Focal Glomerulosclerosis
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Fsgs
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Segmental Glomerulosclerosis
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Glomerulosclerosis, Focal Segmental
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Fgs
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Focal Glomerular Sclerosis
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Familial Idiopathic Nephrotic Syndrome
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Focal Sclerosis With Hyalinosis
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Glomerulosclerosis, Focal
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Glomerulosclerosis Focal
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Glomerulosclerosis, Segmental, Focal
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Focal Segmental Glomerulosclerosis, Not Otherwise Specified
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D-Minus Hemolytic Uremic Syndrome |
Atypical Hus
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Atypical Hemolytic Uremic Syndrome
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Hus, Atypical
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Ahus
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Hemolytic Uremic Syndrome, Atypical 1 |
Atypical Hemolytic-Uremic Syndrome
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Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
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Atypical Hemolytic Uremic Syndrome
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Hemolytic Uremic Syndrome, Atypical, Susceptibility To
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Ahus
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AHUS1
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Hemolytic-Uremic Syndrome
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Ahus 1
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Ahus, Susceptibility To, 1
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Hemolytic Uremic Syndrome, Atypical
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Non-Shiga-Like Toxin-Associated Hus
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Non-Stx-Hus
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Nonenteropathic Hus
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Atypical Hus
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Shiga Toxin-Associated Hemolytic Uremic Syndrome
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D+ Hus
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Ehec-Hus
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Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli
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Hemolytic Uremic Syndrome With Diarrhea
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Stec-Hus
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Shiga-Like Toxin-Associated Hus
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Stx-Hus
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Typical Hus
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Typical Hemolytic Uremic Syndrome
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Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies
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Atypical Hus With Anti-Factor H Antibodies
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Ahus With Anti-Factor H Antibodies
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Ahus With Neutralizing Autoantibodies Against Factor H
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Hemolytic Uremic Syndrome Atypical 1
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Atypical Hemolytic Uremic Syndrome With H Factor Anomaly
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D Hus
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Hemolytic-Uremic Syndrome Without Diarrhea
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Hemolytic-Uremic Syndrome, Atypical, Type 1
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Hemolytic Uremic Syndrome, Typical
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Hypertension, Essential |
Essential Hypertension
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Hypertension
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High Blood Pressure
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Hypertension, Essential, Susceptibility To
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Hypertensive Disease
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Primary Hypertension
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EHT
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Hypertension, Salt-Sensitive Essential, Susceptibility To
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Hyperpiesia
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Idiopathic Hypertension
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Hypertensive Disorder
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Hypertension, Essential, Susceptibility To, 3
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Hypertension, Essential 3
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Hypertension, Essential, Salt-Sensitive
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Hypertension, Essential, Susceptibility To, 6
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Hypertension, Essential 6
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Hypertension, Salt-Sensitive Essential
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Hypertension, Susceptibility To
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Hypertension, Essential, Susceptibility To, 4
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Hypertension, Essential 4
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Hypertension, Essential, Susceptibility To, 2
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Hypertension, Essential 2
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Hypertension, Essential, Susceptibility To, 1
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Hypertension, Essential 1
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Hypertension, Essential, Susceptibility To, 5
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Hypertension, Essential 5
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Htn
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Vascular Hypertensive Disorder
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Systemic Primary Arterial Hypertension
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Hbp - [High Blood Pressure]
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Systemic Arterial Hypertensive Disorder
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Elevated Blood Pressure
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Arterial Hypertension Nos
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Hypertension Nos
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Benign Hypertension
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Systemic Arterial Hypertension
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Systemic Hypertension
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Artery Htn
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Benign Htn
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Vascular Htn
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Vascular Hypertension
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Cholesterol Hypertension
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Cholesterol Htn
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Idiopathic Htn
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Malignant Hypertension
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Malignant Htn
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Raised Blood Pressure
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Cardiovascular Hypertension
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Primary Htn - [Hypertension]
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High Arterial Tension
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High Blood Pressure Disorder
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Ht - [Hypertension]
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Htn - [Hypertension]
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Hypertensive Vascular Disease
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Hypertensive Vascular Degeneration
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X-Linked Alport Syndrome-Diffuse Leiomyomatosis |
Xq22.3 Microdeletion Syndrome
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X-Linked Diffuse Leiomyomatosis-Alport Syndrome
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Leiomyomatosis |
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Autosomal Recessive Alport Syndrome |
Alport Syndrome, Recessive Type
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Alport Syndrome, Autosomal Recessive
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Alport Syndrome Autosomal Recessive
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Alport Syndrome Recessive Type
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Nephropathy And Deafness
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Hematuria, Benign Familial |
Benign Familial Hematuria
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BFH
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Thin Membrane Nephropathy
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Tmn
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Thin Basement Membrane Nephropathy
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Thin-Basement-Membrane Nephropathy
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Hematuria, Familial Benign
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Hematuria Benign Familial
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Hematuria, Benign, Familial
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Thin Basement Membrane Disease
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Kidney Disease |
Renal Failure
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Kidney Failure
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Kidney Diseases
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Nephropathy
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Abnormality Of The Kidney
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Impaired Renal Function Disease
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Renal Anomaly
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Kidney Dysfunction
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Renal Disease
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Nephropathies
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Renal Failure Adverse Event
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Abnormal Renal Function
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Glomerulonephritis |
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Leiomyoma |
Leiomyomatous Neoplasm
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Leiomyomatous Tumor
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Leiomyomas
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Fibroid Tumor
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Uterine Fibroids
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Colon Leiomyoma |
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Sensorineural Hearing Loss |
Sensory Hearing Loss
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Sensorineural Deafness
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Sensorineural Hearing Loss Disorder
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Hearing Loss, Sensorineural
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Central Hearing Loss
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High Frequency Deafness
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High Frequency Hearing Loss
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High-Frequency Hearing Loss
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Perceptive Deafness
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Perceptive Hearing Loss
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Perceptive Hearing Loss Or Deafness
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Hearing Loss Sensorineural
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Deafness Sensorineural
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Hearing Loss High-Frequency
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Hearing Loss, Central
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Hearing Loss, High-Frequency
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End Stage Renal Disease |
End Stage Renal Failure
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End-Stage Kidney Disease
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Kidney Failure, Chronic
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Chronic Kidney Disease Stage 5
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Rare Genetic Deafness |
Rare Genetic Hearing Loss
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Pierson Syndrome |
Microcoria-Congenital Nephrotic Syndrome
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Microcoria-Congenital Nephrosis Syndrome
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PIERS
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Microcoria - Congenital Nephrosis
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Microcoria - Congenital Nephrotic Syndrome
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PIERSS
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Deafness, X-Linked 1 |
DFNX1
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Dfn2
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Deafness, X-Linked 2, Sensorineural Congenital
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X-Linked Deafness 1
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X-Linked Sensorineural Congenital Deafness 2
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Deafness, X-Linked, 1
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Congenital Sensorineural Deafness X-Linked 2
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Deafness, X-Linked, Type 1
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Hereditary Elliptocytosis |
Congenital Elliptocytosis
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Ovalocytosis
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Elliptocytosis, Hereditary
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He
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Elliptocytosis Hereditary
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Congenital Ovalocytosis
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Elliptocytosis
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Hereditary Elliptocytosis With Infantile Poikilocytosis
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Hereditary Ovalocytosis
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Oval Erythrocytosis
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He - [Hereditary Elliptocytosis]
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Elliptocytosis Anaemia
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Goodpasture Syndrome |
Anti-Glomerular Basement Membrane Disease
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Anti-Gbm Disease
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Pulmonary Renal Syndrome
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Anti-Glomerular Basement Membrane Antibody Disease
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Glomerulonephritis - Pulmonary Hemorrhage
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Rapidly Progressive Glomerulonephritis With Pulmonary Hemorrhage
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Anti-Gbm Syndrome
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Goodpasture'S Syndrome
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Anti-Basement Membrane Glomerulonephritis
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Porencephaly |
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Autoimmune Disease Of Urogenital Tract |
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Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2 |
Hypophosphatemic Nephrolithiasis/Osteoporosis 2
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NPHLOP2
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Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2
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Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 2
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Anti-Basement Membrane Glomerulonephritis |
Anti-Gbm Glomerulonephritis
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Polycystic Kidney Disease |
Polycystic Kidney Diseases
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Pkd
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Polycystic Renal Disease
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Kidney Disease, Polycystic
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Polycystic Kidney, Autosomal Dominant
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Amme Complex |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis
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ATS-MR
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Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome
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Chromosome Xq22.3 Telomeric Deletion Syndrome
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Amme Syndrome
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Alport Syndrome With Intellectual Disability, Midface Hypoplasia And Elliptocytosis
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Treacher Collins Syndrome 1 |
Treacher Collins Syndrome
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Mandibulofacial Dysostosis
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Treacher Collins-Franceschetti Syndrome
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Tcof
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Tcs
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Mfd1
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Franceschetti-Klein Syndrome
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TCS1
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Franceschetti Syndrome
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Franceschetti-Zwahlen-Klein Syndrome
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Zygoauromandibular Dysplasia
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Treacher-Collins Syndrome
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Mandibulofacial Dysostosis Without Limb Anomalies
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Bilateral And Symmetric Oto-Mandibular Dysplasia
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Deafness, X-Linked 4 |
DFNX4
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Dfn6
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Deafness, Nonsyndromic Sensorineural Progressive 6
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X-Linked Deafness 4
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Deafness, X-Linked 6, Progressive
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Nonsyndromic Sensorineural Progressive Deafness 6
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X-Linked Progressive Deafness 6
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Deafness, X-Linked, 4
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Deafness Nonsyndromic Sensorineural Progressive 6
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Deafness X-Linked 6 Progressive
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Deafness, X-Linked, Type 4
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Deafness, X-Linked 7 |
X-Linked External Auditory Canal Atresia-Dilated Internal Auditory Canal-Facial Dysmorphism Syndrome
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DFNX7
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X-Linked Deafness 7
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Deafness, X-Linked, 7
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Inner Ear Disease |
Labyrinthine Dysfunction
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Diseases Of Inner Ear
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Labyrinthine Disease
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Abnormality Of The Inner Ear
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Labyrinth Diseases
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Labyrinthine Disorder
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Nonfunctioning Labyrinth
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Labyrinthine Loss Of Function
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Labyrinthine Syndrome
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Labyrinthine Disorder Nos
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Auditory System Disease |
Ear Diseases
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Ear And Mastoid Disease
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Familial Nephrotic Syndrome |
Congenital Nephrotic Syndrome
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Nephrosis, Congenital
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Finnish Congenital Nephrotic Syndrome
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X-Linked Nonsyndromic Deafness |
X-Linked Deafness
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Deafness, X-Linked
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Nail-Patella Syndrome |
Turner-Kieser Syndrome
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Onychoosteodysplasia
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Fong Disease
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NPS
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Hereditary Onycho-Osteodysplasia
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Nps1
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Hereditary Onychoostedysplasia
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Iliac Horn Syndrome
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Nail Patella Syndrome
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Turner-Kiser Syndrome
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Arthro-Onychodysplasia
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Nps 1
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Osteo-Onychodysplasia
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Hereditary Osteo-Onychodysplasia
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Osterreicher Syndrome
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Pelvic Horn Syndrome
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Österreicher-Turner Syndrome
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Nps - [Nail-Patella Syndrome]
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Hood - [Hereditary Onycho-Osteodysplasia] Syndrome
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3-Methylcrotonyl-Coa Carboxylase 2 Deficiency |
MCC2D
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Mcc2 Deficiency
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3-Methylcrotonyl Coa Carboxylase 2 Deficiency
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3-Methylcrotonylglycinuria Ii
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Methylcrotonylglycinuria, Type Ii
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3-Methylcrotonoyl-Coa Carboxylase 2 Deficiency
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3-Methylcrotonylglycinuria Type Ii
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Mcgii
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Methylcrotonylglycinuria Type Ii
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Deafness, X-Linked 2 |
Progressive Deafness With Stapes Fixation
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DFNX2
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Dfn3
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Nance Deafness
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Perilymphatic Gusher-Deafness Syndrome
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Stapedo-Vestibular Ankylosis
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Sensorineural Deafness, Profound, With Or Without A Conductive Component, Associated With A Unique Developmental Abnormality Of The Ear
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X-Linked Deafness 2
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X-Linked Mixed Conductive And Neurosensory Deafness
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X-Linked Mixed Conductive And Sensorineural Deafness
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Deafness 3 Conductive With Stapes Fixation
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Deafness Conductive With Stapes Fixation
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Deafness Mixed With Perilymphatic Gusher
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Thies-Reis Syndrome
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Deafness, Conductive, With Stapes Fixation
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Deafness 3, Conductive, With Stapes Fixation
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Deafness, Mixed, With Perilymphatic Gusher
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Conductive Deafness 3 With Stapes Fixation
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Conductive Deafness With Stapes Fixation
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Mixed Deafness With Perilymphatic Gusher
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X-Linked Deafness Type 2
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X-Linked Mixed Conductive And Neurosensory Hearing Loss
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X-Linked Mixed Conductive And Sensorineural Hearing Loss
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X-Linked Sensorineural Deafness
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X-Linked Stapes Gusher Syndrome
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Deafness Mixed With Perilymphatic Gusher, X-Linked
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Dfn 3 Nonsyndromic Hearing Loss And Deafness
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Gusher Syndrome
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Thies Reis Syndrome
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Progressive Hearing Loss With Stapes Fixation
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Deafness, X-Linked, 2
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Deafness Mixed With Perilymph Gusher X-Linked
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Deafness, X-Linked, Type 2
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Progressive Hearing Loss Stapes Fixation
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Stickler Syndrome |
Arthroophthalmopathy
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Hereditary Arthro-Ophthalmo-Dystrophy
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Hereditary Arthro-Ophthalmopathy
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Stickler Dysplasia
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Hereditary Progressive Arthroophthalmopathy
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Stickler Syndrome, Type 1
|
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Branchiootorenal Syndrome |
Branchio-Oto-Renal Syndrome
|
Bor Syndrome
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Branchiootorenal Dysplasia
|
Melnick-Fraser Syndrome
|
Branchiootorenal Spectrum Disorders
|
Branchio-Otorenal Dysplasia
|
Branchio Oto Renal Syndrome
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Branchiootorenal/Branchiootic Syndrome
|
Bo Syndrome
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Bor
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Bos
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Branchio-Otorenal Syndrome
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Branchiootic Syndrome
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Branchiootorenal Syndrome
|
Branchiootic Syndrome 1
|
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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
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Polycystic Kidney Disease, Autosomal Dominant
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Kidney, Polycystic, Disease, Autosomal Dominant
|
Adult Polycystic Kidney Disease
|
Polycystic Kidney, Adult Type
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Apckd - [Autosomal Polycystic Kidney Disease]
|
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Norrie Disease |
Atrophia Bulborum Hereditaria
|
Episkopi Blindness
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Pseudoglioma
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ND
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Norrie-Warburg Disease
|
Anderson-Warburg Syndrome
|
Fetal Iritis Syndrome
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Norrie Syndrome
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Norrie-Warburg Syndrome
|
Ndp
|
Congenital Progressive Oculo-Acoustico-Cerebral Degeneration
|
Norrie'S Disease
|
Oligophrenia Microphthalmus
|
Pseudoglioma Congenita
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Whitnall-Norman Syndrome
|
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Cakut |
Renal Or Urinary Tract Malformation
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Congenital Anomalies Of Kidney And Urinary Tract
|
Congenital Anomaly Of Kidney And Urinary Tract
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Congenital Anomalies Of The Kidney And Urinary Tract
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Kidney And Urinary Tract, Anomalies, Congenital
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Renal Hypodysplasia, Nonsyndromic, 1
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