| 疾病名称 |
别名 |
|
| Osteomalacia |
|
|
| Hypophosphatemia |
|
Vitamin D-Resistant Rickets
|
Hereditary Hypophosphatemic Rickets
|
|
Vdrr
|
Vitamin D Resistant Rickets
|
|
Hypophosphatemic Rickets, X-Linked Dominant
|
Familial Hypophosphatemic Rickets
|
|
|
| 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
|
|
|
| Rickets |
|
Vitamin D Deficiency
|
Vitamin D
|
|
Active Rickets
|
Hypovitaminosis D
|
|
Nutritional Rickets
|
Vitamin D Deficiency Disease
|
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Vitamin-D Deficiency Rickets
|
Vitamin D-Dependent Rickets
|
|
Avitaminosis D
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Infantile Osteomalacia
|
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Juvenile Osteomalacia
|
|
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| Dentin Dysplasia |
|
Dentinal Dysplasia
|
Dd
|
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Dysplasia, Dentin
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Shell Teeth
|
|
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| Dentinogenesis Imperfecta |
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Hereditary Opalescent Dentin
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Dentinogenesis Imperfecta Without Osteogenesis Imperfecta
|
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Dgi
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Capdepont Teeth
|
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Dgi Without Oi
|
Di
|
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Non-Syndromic Dgi
|
Non-Syndromic Dentinogenesis Imperfecta
|
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Opalescent Teeth Without Oi
|
Opalescent Teeth Without Osteogenesis Imperfecta
|
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Opalescent Dentin
|
|
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| Autosomal Recessive Hypophosphatemic Rickets |
|
Arhr
|
Hypophosphatemic Rickets, Autosomal Recessive
|
|
Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets
|
|
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| Calcinosis |
|
Pathologic Calcification
|
Pathologically Calcified Structure
|
|
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| 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
|
|
|
| Osteogenesis Imperfecta, Type Vi |
|
OI6
|
Osteogenesis Imperfecta Type 6
|
|
Osteogenesis Imperfecta Type Vi
|
Oi Type Vi
|
|
Oi Type 6
|
Osteogenesis Imperfecta Type
|
|
Serpinfi- Related Osteogenesis Imperfecta
|
Osteogenesis Imperfecta 6
|
|
Oi-Vi
|
|
|
| Dental Abscess |
|
|
| 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
|
|
|
| Phosphorus Metabolism Disease |
|
Phosphorus Metabolism Disorders
|
Disorder Of Phosphorus Metabolism
|
|
Phosphorus Disorder
|
Phosphorus Metabolism Disorder
|
|
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| Otosclerosis |
|
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| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
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Bone Mineral Density Quantitative Trait Locus
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Bmnd
|
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Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
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Osteoporosis, Postmenopausal, Susceptibility
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Bone Mineral Density Variation Qtl, Osteoporosis
|
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OSTEOP
|
Involutional Osteoporosis
|
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Senile Osteoporosis
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Osteoporosis Postmenopausal
|
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Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
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Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
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Type 1 Osteoporosis
|
|
|
| Hermansky-Pudlak Syndrome 6 |
|
HPS6
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial
|
|
Delta Storage Pool Disease
|
Hermansky-Pudlak Syndrome, Type 6
|
|
Platelet Storage Pool Deficiency
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
|
|
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| Serous Labyrinthitis |
|
Acute Serous Labyrinthitis
|
|
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| Pulmonary Alveolar Microlithiasis |
|
|
| Hypophosphatemic Rickets With Hypercalciuria, Hereditary |
|
Hereditary Hypophosphatemic Rickets With Hypercalciuria
|
HHRH
|
|
Hypophosphatemic Rickets With Hypercalciuria
|
Hypercalciuric Rickets
|
|
|
| Enthesopathy |
|
|
| Osteoglophonic Dysplasia |
|
Osteoglophonic Dwarfism
|
OGD
|
|
Fairbank-Keats Syndrome
|
Osteoglosphonic Dysplasia
|
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Dysplasia, Osteoglophonic
|
|
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| Osteoblastoma |
|
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| Schimmelpenning-Feuerstein-Mims Syndrome |
|
Nevus Sebaceus Of Jadassohn
|
Organoid Nevus Phakomatosis
|
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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
|
|
|
| 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
|
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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
|
|
|
| Ossifying Fibroma |
|
Peripheral Ossifying Fibroma
|
Fibro-Osteoma
|
|
Fibroma Ossifying
|
Fibroma, Ossifying
|
|
|
| Dental Pulp Necrosis |
|
Pulp Necrosis
|
Necrotic Pulp
|
|
Necrosis Of The Pulp
|
Dead Pulp
|
|
Devitalised Pulp
|
Putrescent Pulpitis
|
|
Devitalized Tooth
|
Dental Pulp Gangrene
|
|
Pulp Gangrene
|
Nonvital Tooth
|
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Pulpless Tooth
|
Putrescent Pulp
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| 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
|
|
|
| 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
|
|
|
| Sclerosteosis |
|
Cortical Hyperostosis With Syndactyly
|
Sost
|
|
Cortical Hyperostosis-Syndactyly Syndrome
|
|
|
| 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
|
|
|
| Bone Remodeling Disease |
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
