| 疾病名称 |
别名 |
|
| Hypophosphatemic Rickets, Autosomal Dominant |
|
Autosomal Dominant Hypophosphatemic Rickets
|
ADHR
|
|
Autosomal Dominant Hypophosphatemia
|
Vitamin D-Resistant Rickets, Autosomal Dominant
|
|
Hypophosphatemia, Autosomal Dominant
|
Autosomal Dominant Vitamin D-Resistant Rickets
|
|
Rickets, Hypophosphatemic, Autosomal Dominant
|
|
|
| Tumoral Calcinosis, Hyperphosphatemic, Familial, 2 |
|
|
| Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 |
|
Hyperphosphatemic Familial Tumoral Calcinosis
|
Hftc
|
|
Hyperostosis-Hyperphosphatemia Syndrome
|
Familial Hyperphosphatemic Tumoral Calcinosis/Hyperphosphatemic Hyperostosis Syndrome
|
|
Tumoral Calcinosis, Hyperphosphatemic, Familial
|
Phptc
|
|
Lipocalcinogranulomatosis
|
Morbus Teutschlaender
|
|
Hhs
|
Hyperostosis With Hyperphosphatemia
|
|
Cortical Hyperostosis With Hyperphosphatemia
|
Primary Hyperphosphatemic Tumoral Calcinosis
|
|
Familial Tumoral Calcinosis
|
HFTC1
|
|
Hypercalcemic Tumoral Calcinosis
|
Hyperphosphatemia Hyperostosis
|
|
Hyperphosphatemia Hyperostosis Syndrome
|
Hyperphosphatemia Tumoral Calcinosis
|
|
Tumoral Calcinosis
|
Calcinosis, Tumoral, With Hyperphosphatemia
|
|
Tumoral Calcinosis, Primary Hyperphosphatemic
|
Teutschlaender Disease, Familial
|
|
Familial Teutschlaender Disease
|
Tumoral Calcinosis With Hyperphosphatemia
|
|
Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome
|
Ftc/Hhs
|
|
Familial Tumoral Calcinosis With Hyperphosphatemia
|
Teutschlaender Disease
|
|
Tumoral Calcinosis Primary Hyperphosphatemic
|
Calcinosis, Tumoral, Hyperphosphatemic, Familial
|
|
|
| Hypophosphatemic Rickets, X-Linked Recessive |
|
Hypophosphatemic Rickets
|
X-Linked Recessive Hypophosphatemic Rickets
|
|
XLRHR
|
Hypophosphatemic Rickets Disorders
|
|
Rickets Hypophosphatemic
|
Rickets, Hypophosphatemic, X-Linked Recessive
|
|
Familial Hypophosphatemic Rickets
|
|
|
| Hypophosphatemia |
|
Vitamin D-Resistant Rickets
|
Hereditary Hypophosphatemic Rickets
|
|
Vdrr
|
Vitamin D Resistant Rickets
|
|
Hypophosphatemic Rickets, X-Linked Dominant
|
Familial Hypophosphatemic Rickets
|
|
|
| Hyperphosphatemia |
|
|
| Rickets |
|
Vitamin D Deficiency
|
Vitamin D
|
|
Active Rickets
|
Hypovitaminosis D
|
|
Nutritional Rickets
|
Vitamin D Deficiency Disease
|
|
Vitamin-D Deficiency Rickets
|
Vitamin D-Dependent Rickets
|
|
Avitaminosis D
|
Infantile Osteomalacia
|
|
Juvenile Osteomalacia
|
|
|
| Calcinosis |
|
Pathologic Calcification
|
Pathologically Calcified Structure
|
|
|
| Osteomalacia |
|
|
| Fibrous Dysplasia |
|
Fibrous Dysplasia Of Bone
|
|
|
| Hyperostosis |
|
Hypertrophy Of Bone
|
Bone Hypertrophy
|
|
Bone Thickening
|
Periosteum Thickening
|
|
|
| Calciphylaxis |
|
|
| Secondary Hyperparathyroidism |
|
Hyperparathyroidism Secondary
|
Hyperparathyroidism, Secondary
|
|
Secondary Hyperparathyroidism Nec
|
|
|
| Renal Osteodystrophy |
|
Renal Rickets
|
Chronic Kidney Disease-Mineral And Bone Disorder
|
|
|
| Paraneoplastic Syndromes |
|
|
| Phosphorus Metabolism Disease |
|
Phosphorus Metabolism Disorders
|
Disorder Of Phosphorus Metabolism
|
|
Phosphorus Disorder
|
Phosphorus Metabolism Disorder
|
|
|
| Hyperparathyroidism |
|
Hyperparathyroidism And Other Disorders Of Parathyroid Gland
|
Parathyroid Hyperfunction
|
|
Hpth - [Hyperparathyroidism]
|
Parathyroid Gland Hyperfunction
|
|
Parathyroid Glandular Hyperfunction
|
|
|
| Arterial Calcification Of Infancy |
|
Idiopathic Infantile Arterial Calcification
|
Generalized Arterial Calcification Of Infancy
|
|
Iiac
|
Occlusive Infantile Arteriopathy
|
|
Infantile Arteriosclerosis
|
Gaci
|
|
Idiopathic Obliterative Arteriopathy
|
Generalized Arterial Calcification In Infancy
|
|
Arteriopathia Calcificans Infantum
|
Diffuse Arterial Calcifying Elastopathy Of Infancy
|
|
Infantile Calcifying Arteriopathy
|
Medial Coronary Sclerosis Of Infancy
|
|
Coronary Sclerosis, Medial, Of Infancy
|
Calcification, Arterial, Generalized, Infancy
|
|
|
| Hypoparathyroidism |
|
Hypoparathyroidism, Idiopathic
|
Parathyroid, Underactivity Of
|
|
Syndrome With Hypoparathyroidism
|
Deficiency Of Parathyroid Hormone
|
|
Parathyroid Gland Insufficiency
|
Parathyroid Insufficiency
|
|
Hypoparathyroidism Due To Impaired Pth - [Parathyroid Hormone] Secretion
|
|
|
| Hypophosphatasia |
|
Phosphoethanolaminuria
|
Childhood Hypophosphatasia
|
|
Deficiency Of Alkaline Phosphatase
|
Hypophospatasia, Childhood
|
|
Hypophosphatasia Mild
|
Phosphoethanol-Aminuria
|
|
Rathburn Disease
|
Hpp
|
|
Rathbun Disease
|
Hypophosphatasia, Childhood
|
|
Infantile Hypophosphatasia
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| 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
|
|
|
| Hypocalcemia, Autosomal Dominant 1 |
|
Autosomal Dominant Hypocalcemia
|
Autosomal Dominant Hypocalcemia 1
|
|
HYPOC1
|
Hypocalcemia, Autosomal Dominant
|
|
Hypercalciuric Hypocalcemia
|
Hypocalcemia, Autosomal Dominant, With Bartter Syndrome
|
|
Familial Hypocalcemia
|
Hypocalcemia, Familial
|
|
Hypoc
|
Adh
|
|
Autosomal Dominant Hypoparathyroidism
|
Familial Hypercalciuric Hypocalcemia
|
|
Ad Hypocalcemia
|
Autosomal Dominant Hypocalcemia With Bartter Syndrome
|
|
Hypoparathyroidism - Autosomal Dominant
|
Hypocalcemia
|
|
|
| Primary Hyperparathyroidism |
|
Familial Primary Hyperparathyroidism
|
Hyperparathyroidism, Primary
|
|
Hyperparathyroidism Primary
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
Familial Benign Hypercalcemia
|
Familial Hyperparathyroidism
|
|
Parathyroid Enlargement
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| Bone Disease |
|
Bone Diseases
|
Skeletal Disease
|
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
| Dental Abscess |
|
|
| Enthesopathy |
|
|
| Nevus, Epidermal |
|
Epidermal Nevus
|
Woolly Hair Nevus
|
|
Epidermal Naevus
|
Epidermal Nevus Syndrome
|
|
Nevus, Keratinocytic, Nonepidermolytic
|
Epidermal Nevus, Somatic
|
|
Nevus, Epidermal, Somatic
|
Nevus Sebaceous Or Woolly Hair Nevus, Somatic
|
|
Nonepidermolytic Keratinocytic Nevus
|
Epidermal Hamartoma Syndrome
|
|
Wooly Hair Nevus
|
Keratinocytic Non-Epidermolytic Nevus
|
|
KNEN
|
Pigmented Moles
|
|
Organoid Nevus Phakomatosis
|
Nevus Sebaceous
|
|
Melanocytic Nevus
|
Melanocytic Nevus Of Skin
|
|
|
| Hypophosphatemic Rickets, X-Linked Dominant |
|
X-Linked Hypophosphatemia
|
Xlh
|
|
Vitamin D-Resistant Rickets, X-Linked
|
X-Linked Hypophosphatemic Rickets
|
|
XLHR
|
Hyp
|
|
Hypophosphatemic Vitamin D-Resistant Rickets
|
Hpdr
|
|
X-Linked Dominant Hypophosphatemic Rickets
|
Familial Hypophosphatemic Rickets
|
|
Hypophosphatemia, X-Linked
|
Hypophosphatemia, Vitamin D-Resistant Rickets
|
|
Hypophosphatemic Rickets X-Linked Dominant
|
X-Linked Vitamin D-Resistant Rickets
|
|
Hypophophatemia, X-Linked
|
Hypophophatemic Vitamin D-Resistant Rickets
|
|
Hypophosphatemia X-Linked
|
Vitamin D-Resistant Rickets X-Linked
|
|
Vitamin D-Resistant Rickets
|
Rickets, X-Linked Hypophosphatemic
|
|
|
| Hypophosphatemic Rickets With Hypercalciuria, Hereditary |
|
Hereditary Hypophosphatemic Rickets With Hypercalciuria
|
HHRH
|
|
Hypophosphatemic Rickets With Hypercalciuria
|
Hypercalciuric Rickets
|
|
|
| Autosomal Recessive Hypophosphatemic Rickets |
|
Arhr
|
Hypophosphatemic Rickets, Autosomal Recessive
|
|
Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets
|
|
|
| Hypervitaminosis D |
|
Vitamin D Hyperalimentation
|
|
|
| Cystinosis |
|
Cystine Storage Disease
|
Cystine Diathesis
|
|
Cystine Disease
|
Cystinoses
|
|
Protein Defect Of Cystin Transport
|
Cystin Transport, Protein Defect Of
|
|
Nephropathic Cystinosis
|
Protein Defect Of Cystine Transport
|
|
|
| Osteoglophonic Dysplasia |
|
Osteoglophonic Dwarfism
|
OGD
|
|
Fairbank-Keats Syndrome
|
Osteoglosphonic Dysplasia
|
|
Dysplasia, Osteoglophonic
|
|
|
| Uremia |
|
|
| Nephrolithiasis |
|
Kidney Stones
|
Stone - Kidney/Ureter
|
|
Kidney Calculi
|
|
|
| Parathyroid Gland Disease |
|
Parathyroid Diseases
|
Disease Of Parathyroid Glands
|
|
Parathyroid Disease
|
|
|
| Metaphyseal Chondrodysplasia, Jansen Type |
|
Metaphyseal Chondrodysplasia, Murk Jansen Type
|
Jansen'S Metaphyseal Chondrodysplasia
|
|
MCDJ
|
Murk Jansen Type Metaphyseal Chondrodysplasia
|
|
Jansen Type Metaphyseal Chondrodysplasia
|
Jansen Disease
|
|
Jansen Metaphyseal Chondrodysplasia
|
Jansen Metaphyseal Dysostosis
|
|
Metaphyseal Chondrodysplasia Murk Jansen Type
|
Chondrodysplasia, Metaphyseal, Murk Jansen Type
|
|
|
| Benign Giant Cell Tumor |
|
|
| Schimmelpenning-Feuerstein-Mims Syndrome |
|
Nevus Sebaceus Of Jadassohn
|
Organoid Nevus Phakomatosis
|
|
Linear Nevus Sebaceous Syndrome
|
Sfm Syndrome
|
|
Jadassohn Nevus Phakomatosis
|
Jnp
|
|
Schimmelpenning Syndrome
|
Solomon Syndrome
|
|
SFM
|
Linear Sebaceous Nevus Syndrome
|
|
Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic
|
Nevus Sebaceus Syndrome
|
|
Organoid Nevus Syndrome
|
Schimmelpenning Feuerstein Mims Syndrome
|
|
Sebaceous Nevus Syndrome, Linear
|
Epidermal Nevus Syndrome, Formerly
|
|
Sebaceous Nevus Syndrome Linear
|
Linear Nevus Sebaceus Syndrome
|
|
Epidermal Nevus Syndrome
|
Ss
|
|
Nevus Sebaceous
|
|
|
| Mesenchymal Cell Neoplasm |
|
Benign Miscellaneous Mesenchymal Tumor
|
Mesenchymal Tumor
|
|
Mesenchymal Tumors
|
|
|
| Ankylosing Spondylitis 1 |
|
Ankylosing Spondylitis, Susceptibility To, 1
|
|
|
| Vitamin D-Dependent Rickets |
|
|
| Skin Atrophy |
|
Atrophic Condition Of Skin
|
Atrophoderma
|
|
Atrophy - Skin
|
|
|
| Vitamin D Hydroxylation-Deficient Rickets, Type 1a |
|
Vitamin D-Dependent Rickets, Type 1a
|
Vitamin D-Dependent Rickets, Type 1
|
|
VDDR1A
|
25-Hydroxycholecalciferol-1-Hydroxylase Deficiency
|
|
1-Alpha-Hydroxylase Deficiency
|
Vdd1
|
|
Pddr1a
|
Pddr Ia
|
|
Vitamin D-Dependent Rickets, Type I
|
Vitamin D-Dependent Rickets Type 1a
|
|
1-Alpha, 25-Hydroxyvitamin D3 Deficiency, Selective
|
Vitamin D Dependency, Type 1
|
|
Pseudovitamin D-Deficiency Rickets, Type Ia
|
Rickets Vitamin D-Dependent 1a
|
|
1-Alpha 25-Hydroxyvitamin D3 Deficiency Selective
|
Pddr
|
|
Pseudovitamin D Deficiency Rickets
|
Pseudovitamin D-Deficiency Rickets Type Ia
|
|
Vitamin D Dependency Type 1
|
|
|
| Blount'S Disease |
|
Blount Disease
|
Tibia Vara
|
|
Osteochondrosis Deformans Tibiae
|
Osteochondrosis Deformans Tibiae, Familial Infantile Type
|
|
Familial Infantile Type Osteochondrosis Deformans Tibiae
|
Blount-Barber Syndrome
|
|
Erlacher-Blount Syndrome
|
Infantile Tibia Vara
|
|
Tibia Vara Blount
|
Blount Disease, Infantile
|
|
|
| Pulmonary Alveolar Microlithiasis |
|
|
| Bone Remodeling Disease |
|
|
| 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
|
|
|
| Osteitis Fibrosa |
|
Osteitis Fibrosa Cystica
|
Hyperparathyroid Bone Disease
|
|
Osteitis Fibrosa Cystica Generalisata
|
Von Recklinghausen'S Bone Disease
|
|
Osteitis Fibrosa Disseminata
|
|
|
| Vitamin D Hydroxylation-Deficient Rickets, Type 1b |
|
VDDR1B
|
Vitamin D-Dependent Rickets Type 1b
|
|
Vitamin D-Dependent Rickets, Type 1b
|
25-Hydroxyvitamin D3 Deficiency, Selective
|
|
Pseudovitamin D3 Deficiency Rickets Due To 25-Hydroxylase Deficiency
|
Rickets Due To Defect In Vitamin D 25-Hydroxylation Deficiency
|
|
Rickets Vitamin D-Dependent 1b
|
25-Hydroxyvitamimn D3 Deficiency Selective
|
|
25-Hydroxyvitamin D(3) Deficiency
|
Pseudovitamin D(3) Deficiency Rickets Due To 25-Hydroxylase Deficiency
|
|
Selective 25-Hydroxyvitamin D(3) Deficiency
|
Rickets Due To Defect In Vitamin D 25-Hydroxylation
|
|
|
| Vitamin D-Dependent Rickets Type 2b |
|
|
| 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
|
|
|
| Osteoblastoma |
|
|
| Ossifying Fibroma |
|
Peripheral Ossifying Fibroma
|
Fibro-Osteoma
|
|
Fibroma Ossifying
|
Fibroma, Ossifying
|
|
|
| Nephrolithiasis/Osteoporosis, Hypophosphatemic, 1 |
|
Hypophosphatemic Nephrolithiasis/Osteoporosis 1
|
NPHLOP1
|
|
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
|
Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 1
|
|
|
| Lacrimoauriculodentodigital Syndrome |
|
Ladd Syndrome
|
Levy-Hollister Syndrome
|
|
Lacrimo-Auriculo-Dento-Digital Syndrome
|
LADD
|
|
Lacrimoauriculodento-Digital Syndrome
|
Levy Hollister Syndrome
|
|
Lard Syndrome
|
Lacrimoauriculoradiodental Syndrome
|
|
LADDS
|
Congenital Duodenal Obstruction Due To Malrotation Of Intestine
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Vitamin D-Dependent Rickets, Type 2a |
|
Hvdrr
|
Generalized Resistance To 1,25-Dihydroxyvitamin D
|
|
Hypocalcemic Vitamin D-Resistant Rickets
|
VDDR2A
|
|
Rickets, Hereditary Vitamin D-Resistant
|
Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol
|
|
Pddr Iia
|
Rickets-Alopecia Syndrome
|
|
Rickets, Vitamin D-Resistant, Type Iia
|
Vitamin D-Dependent Rickets Type 2a
|
|
Vitamin D-Dependent Rickets, Type 2
|
Vitamin D-Dependent Rickets, Type 2a, With Or Without Alopecia
|
|
Generalized 1,25-Dihydroxyvitamin D
|
Pseudovitamin D-Deficiency, Type Iia
|
|
Hereditary Vitamin D-Resistant Rickets
|
Vddr Ii
|
|
Vdrr Ii
|
Vitamin D-Dependent Rickets Type Ii
|
|
Vitamin D-Resistant Rickets Type Ii
|
Rickets Vitamin D-Dependent 2a
|
|
Pseudovitamin D-Deficiency Type Iia
|
Rickets Hereditary Vitamin D-Resistant
|
|
Type Iia Rickets
|
Vitamin D-Dependent Rickets Type 2a With Or Without Alopecia
|
|
Vitamin D-Dependent Rickets, Type Ii
|
Familial Hypophosphatemic Rickets
|
|
Hypophosphatemic Rickets, X-Linked Dominant
|
|
|
| Metaphyseal Dysplasia |
|
Bakwin-Krida Syndrome
|
Pyle'S Disease
|
|
Pyle-Cohn Syndrome
|
|
|
| Polycystic Kidney Disease 4 |
|
|
| Fanconi Syndrome |
|
Infantile Nephropathic Cystinosis
|
Adult Fanconi Syndrome
|
|
Congenital Fanconi Syndrome
|
De Toni-Fanconi Syndrome
|
|
Fanconi-De Toni Syndrome
|
Lignac-Fanconi Syndrome
|
|
Fanconi Renotubular Syndrome
|
Primary Fanconi Renotubular Syndrome
|
|
De Toni-Debre-Fanconi Syndrome
|
Adult Fanconi Anemia
|
|
Detoni Fanconi Syndrome
|
Fanconi-De-Toni Syndrome
|
|
Primary Fanconi Syndrome
|
Detoni-Debre-Fanconi Syndrome
|
|
Primary Fanconi Renal Syndrome
|
Fanconi Anemia
|
|
Cystinosis, Infantile Nephropathic
|
Fanconi-Bickel Syndrome
|
|
Renal Fanconi Syndrome
|
Lowe-Bickel Syndrome
|
|
|
| Microcephaly And Chorioretinopathy 1 |
|
|
| Bone Benign Neoplasm |
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Acquired Metabolic Disease |
|
|
| Bone Resorption Disease |
|
|
| Conjunctival Deposit |
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Diabetes Mellitus |
|
|
| 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]
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Crouzon Syndrome |
|
Crouzon Craniofacial Dysostosis
|
Craniofacial Dysostosis
|
|
Cfd1
|
Craniofacial Dysostosis Type 1
|
|
Crouzon Disease
|
Crouzon'S Disease
|
|
Craniofacial Dysostosis, Type I
|
Craniofacial Dysarthrosis
|
|
Craniofacial Dysostosis Syndrome
|
CS
|
|
Craniofacial Dysostosis Type I
|
Vogt Cephalosyndactyly
|
|
|
| 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
|
|
|
| Cystic Kidney Disease |
|
Renal Cyst
|
Simple Renal Cyst
|
|
Kidney Cysts
|
Kidney Diseases, Cystic
|
|
Renal Cysts
|
Kidney Cyst
|
|
Cystic Kidney
|
Congenital Cystic Kidney Disease
|
|
Cystic Kidney Diseases
|
Bosniak 1 Cyst
|
|
|
| Hyperlipoproteinemia, Type V |
|
Hyperlipoproteinemia Type V
|
Hyperchylomicronemia, Late-Onset
|
|
Familial Type 5 Hyperlipoproteinemia
|
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
|
|
Hyperlipidemia, Type V
|
Hyperlipemia, Mixed
|
|
Hyperlipemia, Combined Fat And Carbohydrate-Induced
|
Familial Hyperlipoproteinemia Type V
|
|
Fredrickson Type V Lipaemia
|
Hyperlipoproteinemia Type 5
|
|
Hyperchylomicronemia Late Onset
|
Hyperlipemia Combined Fat And Carbohydrate-Induced
|
|
Hyperlipemia Mixed
|
Hyperlipidemia Type V
|
|
Mixed Hyperlipemia
|
Type V Hyperlipoproteinemia
|
|
Hyperlipoproteinemia 5
|
HLPP5
|
|
Hyperlipidemia, Familial Combined
|
Mixed Hyperlipidemia
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| 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
|
|
|
| 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 Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
