| 疾病名称 |
别名 |
|
| Gitelman Syndrome |
|
Familial Hypokalemia-Hypomagnesemia
|
Hypomagnesemia-Hypokalemia, Primary Renotubular, With Hypocalciuria
|
|
Potassium And Magnesium Depletion
|
GTLMNS
|
|
Gitelman'S Syndrome
|
Gs
|
|
Hypokalemia-Hypomagnesemia, Primary Renotubular, With Hypocalciuria
|
Tubular Hypomagnesemia-Hypokalemia With Hypocalcuria
|
|
Bartter Syndrome Gitelman Variant
|
Bartter Syndrome Hypocalciuric Variant
|
|
Primary Renotubular Hypomagnesemia-Hypokalemia With Hypocalciuria
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Bartter Disease |
|
Bartter Syndrome
|
Bartter'S Syndrome
|
|
Aldosteronism With Hyperplasia Of The Adrenal Cortex
|
Hypokalemic Alkalosis With Hypercalciuria
|
|
Potassium Wasting
|
Juxtaglomerular Hyperplasia With Secondary Aldosteronism
|
|
Renal Tubular Normotensive Hypokalemic Alkalosis With Hypercalciuria
|
Salt-Losing Tubular Disorder, Henle'S Loop Type
|
|
Salt-Wasting Tubulopathy, Henle'S Loop Type
|
Bartters Syndrome
|
|
|
| Chondrocalcinosis |
|
Pseudogout
|
Calcium Pyrophosphate Deposition Disease
|
|
Familial Chondrocalcinosis
|
Chondrocalcinosis Nos
|
|
Cppd - [Calcium Pyrophosphate Deposition Disease]
|
Cpdd - [Calcium Pyrophosphate Deposition Disease]
|
|
Chondrocalcinosis, Due To Pyrophosphate Crystals, Involving Unspecified Site
|
Chondrocalcinosis, Cause Unspecified
|
|
Chondrocalcinosis Due To Pyrophosphate Crystals
|
Chondrocalcinosis Articularis
|
|
Calcium Pyrophosphate Arthritis And Periarthritis
|
|
|
| Bartter Syndrome, Type 3 |
|
Bartter Disease Type 3
|
BARTS3
|
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Bartter Syndrome Type 3
|
Bartter Syndrome, Classic
|
|
Classic Bartter Syndrome
|
Bartter Syndrome Classic
|
|
Bartter Syndrome Type Iii
|
Bartter Syndrome 3
|
|
|
| Renal Tubular Transport Disease |
|
Renal Tubular Transport, Inborn Errors
|
Inborn Renal Tubular Transport Disorder
|
|
|
| Arthrogryposis, Distal, Type 3 |
|
Gordon Syndrome
|
DA3
|
|
Distal Arthrogryposis Type 3
|
Arthrogryposis Multiplex Congenita, Distal, Type Iia
|
|
Camptodactyly, Cleft Palate, And Clubfoot
|
Camptodactyly-Cleft Palate-Clubfoot Syndrome
|
|
Distal Arthrogryposis Multiplex Congenita Type Iia
|
Arthrogryposis Distal Type 3
|
|
Distal Arthrogryposis Type Iia
|
Arthrogryposis, Distal, 3
|
|
Pseudohypoaldosteronism, Type Ii
|
|
|
| Pseudohypoaldosteronism |
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
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Corticotroph Pituitary Adenoma
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
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Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
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Aldosteronism Primary
|
Acth Syndrome Ectopic
|
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Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
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Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| Nephrocalcinosis |
|
Hypercalcemic Nephropathy
|
|
|
| Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, And Electrolyte Imbalance |
|
Sesame Syndrome
|
East Syndrome
|
|
SESAMES
|
Epilepsy, Ataxia, Sensorineural Deafness And Tubulopathy
|
|
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation And Electrolyte Imbalance
|
Epilepsy-Ataxia-Sensorineural Deafness-Tubulopathy Syndrome
|
|
Seizures-Sensorineural Deafness-Ataxia-Intellectual Disability-Electrolyte Imbalance Syndrome
|
Epilepsy, Ataxia, Sensorineural Deafness, And Tubulopathy
|
|
Seizures - Sensorineural Deafness - Ataxia - Intellectual Disability - Electrolyte Imbalance
|
Epilepsy-Ataxia-Sensorineural Hearing Loss-Tubulopathy Syndrome
|
|
Seizures-Sensorineural Hearing Loss-Ataxia-Intellectual Disability-Electrolyte Imbalance Syndrome
|
Seizures, Sensorineural Deafness, Ataxia, Intellectual Disability, And Electrolyte Imbalance
|
|
Epilepsy Ataxia Sensorineural Deafness And Tubulopathy
|
Seizures, Sensorineural Deafness, Ataxia, Intellectual Disability, And Electrolyte Imbalance Syndrome
|
|
|
| Bartter Syndrome, Type 1, Antenatal |
|
Hyperprostaglandin E Syndrome 1
|
Bartter Disease Type 1
|
|
BARTS1
|
Bartter Syndrome, Type 1
|
|
Bartter Syndrome Type 1
|
Hypokalemic Alkalosis With Hypercalciuria Antenatal 1
|
|
Hypokalemic Alkalosis With Hypercalciuria 1, Antenatal
|
Bartter Syndrome Type 1 Antenatal
|
|
Hypokalemic Alkalosis With Hypercalciuria 1 Antenatal
|
Bartter Syndrome Antenatal Type 1
|
|
Antenatal Bartter Syndrome Type 1
|
Bartter Syndrome Type I
|
|
Bartter Syndrome 1, Antenatal
|
Abs1
|
|
Antenatal Bartter Syndrome 1
|
Bs1
|
|
Bartter Syndrome, Antenatal Type 1
|
Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis
|
|
|
| Pendred Syndrome |
|
Goiter-Deafness Syndrome
|
Deafness With Goiter
|
|
PDS
|
Thyroid Dyshormonogenesis 2b
|
|
Tdh2b
|
Autosomal Recessive Sensorineural Hearing Impairment And Goiter
|
|
Pendred'S Syndrome
|
Thyroid Hormonogenesis, Genetic Defect In, 2b
|
|
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2b
|
Congenital Hypothyroidism Due To Dyshormonogenesis 2b
|
|
Genetic Defect In Thyroid Hormonogenesis 2b
|
Autosomal Recessive Sensorineural Hearing Impairment, Enlarged Vestibular Aqueduct, And Goiter
|
|
Goiter-Hearing Loss Syndrome
|
Goitre-Deafness Syndrome
|
|
Goitre Deafness
|
|
|
| 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
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| Dipsogenic Diabetes Insipidus |
|
Primary Polydipsia
|
Doid:0081058
|
|
Psychogenic Polydipsia
|
|
|
| Thyroid Dyshormonogenesis 6 |
|
TDH6
|
Genetic Defect In Thyroid Hormonogenesis 6
|
|
Thyroid Hormonogenesis, Genetic Defect In, 6
|
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 6
|
|
Chdh6
|
Congenital Hypothyroidism Due To Dyshormonogenesis Type 6
|
|
|
| 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
|
|
|
| Agenesis Of The Corpus Callosum With Peripheral Neuropathy |
|
Andermann Syndrome
|
Charlevoix Disease
|
|
ACCPN
|
Polyneuropathy, Sensorimotor, With Or Without Agenesis Of The Corpus Callosum
|
|
Corpus Callosum, Agenesis Of, With Neuronopathy
|
Corpus Callosum Agenesis-Neuronopathy Syndrome
|
|
Agenesis Of Corpus Callosum With Neuronopathy
|
Agenesis Of Corpus Callosum With Peripheral Neuropathy
|
|
Agenesis Of Corpus Callosum With Polyneuropathy
|
Corpus Callosum Agenesis Neuronopathy
|
|
Hmsn/Acc
|
Hereditary Motor And Sensory Neuropathy With Agenesis Of The Corpus Callosum
|
|
Agenesis Of The Corpus Callosum, With Peripheral Neuropathy
|
Andermann'S Syndrome
|
|
Agenesis, Corpus Callosum, With Peripheral Neuropathy
|
|
|
| Familial Periodic Paralysis |
|
Genetic Periodic Paralysis
|
Paralyses, Familial Periodic
|
|
|
| Hypokalemic Periodic Paralysis, Type 1 |
|
Hypokalemic Periodic Paralysis
|
Hokpp
|
|
Hypopp
|
Westphall Disease
|
|
HOKPP1
|
Familial Hypokalemic Periodic Paralysis
|
|
Familial Periodic Paralysis
|
Westphal Disease
|
|
Hypokalemic Periodic Paralysis Type 1
|
Hypokalemic Familial Periodic Paralysis
|
|
Periodic Hypokalemic Paralysis
|
Periodic Paralysis I
|
|
Hypokpp
|
Primary Hypokalemic Periodic Paralysis
|
|
Periodic Paralysis Hypokalemic 1
|
Paralysis, Hypokalemic, Periodic
|
|
Paralysis, Hypokalemic, Periodic, Type 1
|
|
|
| Apparent Mineralocorticoid Excess |
|
Cortisol 11-Beta-Ketoreductase Deficiency
|
Apparent Mineralocorticoid Excess Syndrome
|
|
AME
|
Ame1
|
|
11-Beta-Hydroxysteroid Dehydrogenase Deficiency Type 2
|
Ulick Syndrome
|
|
Mineralocorticoid Excess Syndrome, Apparent
|
Syndrome Of Apparent Mineralocorticoid Excess
|
|
Ame 1
|
11 Beta Hydroxysteroid Dehydrogenase Type 2 Deficiency
|
|
|
| Liddle Syndrome 1 |
|
Liddle Syndrome
|
Pseudoaldosteronism
|
|
Liddle'S Syndrome
|
LIDLS1
|
|
Lidls
|
Pseudohyperaldosteronism
|
|
Pseudoprimary Hyperaldosteronism
|
Pseudohyperaldosteronism Type 1
|
|
Liddles Syndrome
|
|
|
| Hypomagnesemia 3, Renal |
|
HOMG3
|
Renal Hypomagnesemia 3
|
|
Fhhnc Without Severe Ocular Involvement
|
Renal Hypomagnesemia Type 3
|
|
Hypomagnesemia, Primary, Due To Defect In Renal Tubular Transport Of Magnesium
|
Hypomagnesemia, Isolated Renal
|
|
Hypomagnesemia, Familial, With Hypercalciuria And Nephrocalcinosis
|
Familial Primary Hypomagnesemia With Hypercalciuria And Nephrocalcinosis Without Severe Ocular Involvement
|
|
Isolated Renal Hypomagnesemia
|
Primary Hypomagnesemia Due To Defect In Renal Tubular Transport Of Magnesium
|
|
Primary Hypomagnesemia With Hypercalciuria And Nephrocalcinosis Without Severe Ocular Involvement
|
Hypomagnesemia 3
|
|
Familial Hypomagnesemia With Hypercalciuria And Nephrocalcinosis
|
Fhhnc
|
|
Hhn
|
Renal Hypomagnesemia Hypercalciuria Nephrocalcinosis
|
|
Hypomagnesemia, Type 3, Renal
|
Primary Hypomagnesemia
|
|
|
| Miliaria Rubra |
|
Miliaria
|
Prickly Heat
|
|
Miliaria Crystallina
|
|
|
| Renal Tubular Acidosis |
|
Acidosis Renal Tubular
|
Acidosis, Renal Tubular
|
|
Lightwood-Albright Syndrome
|
Lightwood Syndrome
|
|
Idiopathic Infantile Hypercalcemia - Mild Form
|
Kidney Tubular Acidosis
|
|
Renal Tubule Acidosis
|
Kidney Acidosis
|
|
Renal Acidosis
|
Renal Hyperchloremic Acidosis
|
|
Rta - [Renal Tubular Acidosis]
|
|
|
| Miliaria |
|
Eccrine Miliaria
|
Heat Rash
|
|
Sweat Rash
|
Sweat Retention Syndrome
|
|
|
| Nephrogenic Diabetes Insipidus |
|
Vasopressin-Resistant Diabetes Insipidus
|
Diabetes Insipidus, Nephrogenic
|
|
Diabetes Insipidus Nephrogenic
|
Congenital Nephrogenic Diabetes Insipidus
|
|
Adh Resistant Diabetes Insipidus
|
Diabetes Insipidus Nephrogenic X-Linked
|
|
Diabetes Insipidus Nephrogenic Type 1
|
Adh-Resistant Diabetes Insipidus
|
|
Diabetes Insipidus Renalis
|
Ndi
|
|
Renal Diabetes Insipidus
|
Familial Nephrogenic Diabetes
|
|
Antidiuretic-Hormone-Resistant Diabetes Insipidus
|
Adiuretin-Resistant Diabetes Insipidus
|
|
Ndi - [Nephrogenic Diabetes Insipidus]
|
Diabetes Tenuifluus
|
|
Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus
|
Hereditary Nephrogenic Diabetes Insipidus
|
|
Familial Nephrogenic Diabetes Insipidus
|
Primary Nephrogenic Diabetes Insipidus
|
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| 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
|
|
|
| Polyhydramnios |
|
|
| 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]
|
|
|
| Cakut |
|
Renal Or Urinary Tract Malformation
|
Congenital Anomalies Of Kidney And Urinary Tract
|
|
Congenital Anomaly Of Kidney And Urinary Tract
|
Congenital Anomalies Of The Kidney And Urinary Tract
|
|
Kidney And Urinary Tract, Anomalies, Congenital
|
Renal Hypodysplasia, Nonsyndromic, 1
|
|
|
| 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]
|
|
|
