| 疾病名称 |
别名 |
|
| Metatropic Dysplasia |
|
Metatropic Dwarfism
|
MTD
|
|
Metatropic Dysplasia Type 1
|
Metatropic Dysplasia, Nonlethal Dominant
|
|
|
| Hereditary Motor And Sensory Neuropathy, Type Iic |
|
CMT2C
|
Charcot-Marie-Tooth Disease Axonal Type 2c
|
|
HMSN2C
|
Hmsn Iic
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2c
|
Charcot-Marie-Tooth Neuropathy Type 2c
|
|
Hereditary Motor And Sensory Neuropathy Type Iic
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2c
|
|
Charcot-Marie-Tooth Neuropathy, Type 2c
|
Autosomal Cominant Axonal Charcot-Marie-Tooth Disease Type 2c
|
|
Charcot-Marie-Tooth Disease 2c
|
Charcot-Marie-Tooth Disease Axonal Autosomal Dominant 2c
|
|
Charcot-Marie-Tooth Disease, Type 2c
|
|
|
| Scapuloperoneal Spinal Muscular Atrophy |
|
SPSMA
|
Amyotrophy, Neurogenic Scapuloperoneal, New England Type
|
|
Neurogenic Scapuloperoneal Amyotrophy, New England Type
|
Scapuloperoneal Neuronopathy
|
|
Spinal Muscular Atrophy, Scapuloperoneal
|
Amyotrophy Neurogenic Scapuloperoneal New England Type
|
|
Muscular Atrophy, Spinal
|
Scapuloperoneal Form Of Spinal Muscular Atrophy
|
|
|
| Spondylometaphyseal Dysplasia, Kozlowski Type |
|
Spondylometaphyseal Dysplasia Kozlowski Type
|
Jequier Kozlowski Skeletal Dysplasia
|
|
Smd Kozlowski Type
|
SMDK
|
|
Dysmorphism Arthrogryposis Skeletal Maturation Advanced
|
Jequier-Kozlowski Syndrome
|
|
Skeletal Dysplasia Jequier-Kozlowski Type
|
Smd, Kozlowski Type
|
|
|
| Neuronopathy, Distal Hereditary Motor, Type Viii |
|
Autosomal Dominant Congenital Benign Spinal Muscular Atrophy
|
HMN8
|
|
Dhmn8
|
Neuropathy, Distal Hereditary Motor, Type Viii
|
|
Distal Hereditary Motor Neuronopathy Type 8
|
Autosomal Dominant Benign Distal Spinal Muscular Atrophy
|
|
Congenital Benign Spinal Muscular Atrophy With Contractures
|
Congenital Nonprogressive Spinal Muscular Atrophy
|
|
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive
|
Spinal Muscular Atrophy, Congenital Benign, With Contractures
|
|
Distal Hereditary Motor Neuropathy Type Viii
|
Neuronopathy, Distal Hereditary Motor, 8
|
|
Distal Spinal Muscular Atrophy, Congenital Non-Progressive
|
Spinal Muscular Atrophy Congenital Benign With Contractures
|
|
|
| Parastremmatic Dwarfism |
|
Parastremmatic Dysplasia
|
PSTD
|
|
Dwarfism, Parastremmatic
|
|
|
| Digital Arthropathy-Brachydactyly, Familial |
|
Familial Digital Arthropathy-Brachydactyly
|
FDAB
|
|
|
| Brachyolmia Type 3 |
|
Brachyrachia
|
Autosomal Dominant Brachyolmia
|
|
BCYM3
|
Brachyolmia, Autosomal Dominant
|
|
Brachyolmia Autosomal Dominant
|
Brachyolmia 3
|
|
Brachyolmia, Type 3
|
|
|
| Spondyloepiphyseal Dysplasia, Maroteaux Type |
|
Spondyloepiphyseal Dysplasia Maroteaux Type
|
Pseudo-Morquio Syndrome Type 2
|
|
Sed, Maroteaux Type
|
Brachyolmia Type 2
|
|
Pseudo-Morquio Syndrome, Type 2
|
Spondyloepiphyseal Dysplasia Of Maroteaux
|
|
Brachyolmia Maroteaux Type
|
SEDM
|
|
Sed Maroteaux Type
|
Dysplasia, Spondyloepiphyseal, Maroteaux Type
|
|
|
| Avascular Necrosis Of Femoral Head, Primary, 2 |
|
ANFH2
|
Avascular Necrosis Of The Femoral Head, Primary 2
|
|
|
| Sodium Serum Level Quantitative Trait Locus 1 |
|
Sodium Serum Level Qtl 1
|
SSQTL1
|
|
|
| Trpv4-Related Bone Disorder |
|
|
| Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal |
|
|
| Familial Avascular Necrosis Of The Femoral Head |
|
Familial Osteonecrosis Of The Femoral Head
|
Primary Avascular Necrosis Of The Femoral Head
|
|
Familial Avascular Necrosis Of Femoral Head
|
Avascular Necrosis Of Femoral Head, Primary
|
|
|
| Clubfoot |
|
Congenital Talipes Equinovarus
|
Congenital Clubfoot
|
|
Congenital Equinovarus
|
Equinovarus Deformity Of Foot
|
|
Club Foot
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Talipes Equinovarus |
|
Congenital Equinovarus
|
Congenital Talipes Equinovarus
|
|
Equinovarus
|
Congenital Varus Clubfoot
|
|
|
| Clubfoot, Congenital, With Or Without Deficiency Of Long Bones And/Or Mirror-Image Polydactyly |
|
CCF
|
Familial Clubfoot Due To 5q31 Microdeletion
|
|
Familial Clubfoot Due To Pitx1 Point Mutation
|
Hereditary Clubfoot Due To Pitx1 Point Mutation
|
|
Hereditary Clubfoot Due To 5q31 Microdeletion
|
Talipes Equinovarus
|
|
Tev
|
Clubfoot, Congenital, With/Without Deficiency Of Long Bones And/Or Mirror-Image Polydactyly
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Primary Bone Dysplasia |
|
Primary Osteodysplasia
|
Primary Skeletal Dysplasia
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Beckwith-Wiedemann Syndrome |
|
Wiedemann-Beckwith Syndrome
|
BWS
|
|
Exomphalos-Macroglossia-Gigantism Syndrome
|
Emg Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation
|
Emg Abnormality
|
|
Wbs
|
Exomphalos Macroglossia Gigantism Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation
|
Macroglossia Exomphalos Gigantism
|
|
|
| Brachyolmia |
|
|
| Progressive Muscular Atrophy |
|
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
| Genetic Motor Neuron Disease |
|
Genetic Anterior Horn Cell Disease
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| Arthropathy |
|
Ankylosis Of Ankle And Foot Joint
|
Ankylosis Of Forearm Joint
|
|
Ankylosis Of Hand Joint
|
Ankylosis Of Joint Of Ankle And/Or Foot
|
|
Ankylosis Of Joint Of Forearm
|
Ankylosis Of Joint Of Hand
|
|
Ankylosis Of Joint Of Lower Leg
|
Ankylosis Of Joint Of Multiple Sites
|
|
Ankylosis Of Joint Of Pelvic Region And Thigh
|
Ankylosis Of Joint Of Shoulder Region
|
|
Ankylosis Of Joint Of Upper Arm
|
Ankylosis Of Lower Leg Joint
|
|
Ankylosis Of Multiple Joints
|
Ankylosis Of Upper Arm Joint
|
|
Infectious Arthropathy
|
Joint Ankylosis Of The Ankle And Foot
|
|
Joint Ankylosis Of The Ankle And/Or Foot
|
Joint Ankylosis Of The Forearm
|
|
Joint Ankylosis Of The Hand
|
Joint Ankylosis Of The Lower Leg
|
|
Joint Ankylosis Of The Pelvic Region And Thigh
|
Joint Ankylosis Of The Shoulder Region
|
|
Joint Ankylosis Of The Upper Arm
|
Joint Diseases
|
|
Joint Disease
|
Arthropathy Associated With Infection
|
|
|
| Spondyloepimetaphyseal Dysplasia, Strudwick Type |
|
Spondylometaphyseal Dysplasia
|
Strudwick Syndrome
|
|
Dappled Metaphysis Syndrome
|
Semd, Strudwick Type
|
|
Spondylometaepiphyseal Dysplasia Congenita, Strudwick Type
|
Smed, Strudwick Type
|
|
Smd
|
Smed Strudwick Type
|
|
SEMDSTWK
|
Smed, Type I
|
|
Semdc
|
Smed Type 1
|
|
Spondyloepimetaphyseal Dysplasia Strudwick Type
|
Sed Strudwick
|
|
Spondyloepimetaphyseal Dysplasia Congenita, Strudwick Type
|
Smed Type I
|
|
Spondyloepiphyseal Dysplasia Congenita With Dappled Metaphyses
|
Dysplasia, Spondyloepimetaphyseal, Strudwick Type
|
|
Dysplasia, Spondylometaphyseal
|
|
|
| Muscular Atrophy |
|
Muscle Wasting
|
Amyotrophia
|
|
Wasting - Muscle
|
Skeletal Muscle Atrophy
|
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| Avascular Necrosis |
|
|
| Tooth Disease |
|
Tooth Diseases
|
Teeth Disease
|
|
Tooth Disorders
|
|
|
| Spondyloepimetaphyseal Dysplasia |
|
Dysplasia, Spondyloepimetaphyseal
|
|
|
| Neuropathy |
|
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
| Pulmonary Edema |
|
|
| Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques |
|
Olmsted Syndrome
|
Mutilating Palmoplantar Hyperkeratosis With Periorificial Keratotic Plaques
|
|
Palmoplantar And Periorificial Keratoderma
|
Olms
|
|
|
| Cystitis |
|
Infective Cystitis
|
Urocystitis
|
|
Pyocystitis
|
|
|
| Diabetic Neuropathy |
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
|
Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
|
CMT2S
|
CMT2Y
|
|
Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Disease Type 2y
|
|
Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
|
Charcot-Marie-Tooth Disease, Type 2e
|
Hereditary Motor And Sensory Neuropathy Type 2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
|
Charcot-Marie-Tooth Disease, Axonal, Type 2y
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
|
Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Neuropathy Type 2e
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
|
Charcot-Marie-Tooth Disease Type 2s
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
|
Cmt2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
|
Hereditary Motor And Sensory Neuropathy Okinawa Type
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
|
Charcot-Marie-Tooth Neuropathy Type 2y
|
Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
|
Charcot-Marie-Tooth Neuropathy Type 2s
|
Charcot-Marie-Tooth Type 2
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
|
Charcot-Marie-Tooth Disease 2e
|
|
Charcot-Marie-Tooth Disease Axonal Type 2e
|
Charcot-Marie-Tooth Disease Neuronal Type 2e
|
|
Charcot-Marie-Tooth Disease 2s
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
|
Charcot-Marie-Tooth Disease 2y
|
Charcot-Marie-Tooth Disease, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
|
|
| Brain Edema |
|
Cerebral Edema
|
Intracranial Swelling
|
|
Wet Brain
|
|
|
| Motor Peripheral Neuropathy |
|
Motor Neuritis
|
Peripheral Motor Neuropathy
|
|
Hereditary Motor And Sensory Neuropathy
|
Hsmn
|
|
Hsmn - Hereditary Sensory And Motor Neuropathy
|
Neuropathic Muscular Atrophy
|
|
Hereditary Sensory And Motor Neuropathy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Familial Episodic Pain Syndrome |
|
|
| Photoparoxysmal Response 1 |
|
Photosensitivity Disease
|
Photodermatitis
|
|
Photosensitivity Disorders
|
PPR1
|
|
Ppr
|
Photosensitivity
|
|
Photoconvulsive Reaction
|
Epilepsy, Photogenic
|
|
Photosensitivity Of Skin
|
Dermatitis, Phototoxic
|
|
|
| Brachydactyly |
|
|
| Megalencephalic Leukoencephalopathy With Subcortical Cysts |
|
Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
Mlc
|
|
Van Der Knaap Disease
|
Lvm
|
|
Leukoencephalopathy With Swelling And Cysts
|
Megalencephaly-Cystic Leukodystrophy
|
|
Megalencephalic Leukodystrophy Megalencephaly-Cystic Leukodystorphy Syndrome
|
Infantile Leukoencephalopathy And Megalencephaly
|
|
Leukoencephalopathy With Swelling And A Discrepantly Mild Course
|
Vacuolating Leukoencephalopathy
|
|
Megalencephalic Leukodystrophy
|
Megalencephaly-Cystic Leukodystrophy Syndrome
|
|
Van Der Knaap Syndrome
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts
|
|
|
| Neuromyotonia And Axonal Neuropathy, Autosomal Recessive |
|
Gamstorp-Wohlfart Syndrome
|
Autosomal Recessive Axonal Neuropathy With Neuromyotonia
|
|
NMAN
|
Myokymia, Myotonia, And Muscle Wasting
|
|
Aran-Nm
|
Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 With Neuromyotonia
|
|
Autosomal Recessive Neuromyotonia And Axonal Neuropathy
|
Arcmt2-Nm
|
|
Myokymia, Myotonia And Muscle Wasting
|
Myokymia Myotonia And Muscle Wasting
|
|
Isaacs Syndrome
|
|
|
| Oculoectodermal Syndrome |
|
Aplasia Cutis Congenita With Epibulbar Dermoids
|
Toriello-Lacassie-Droste Syndrome
|
|
Oculoectodermal Syndrome, Somatic
|
OES
|
|
Aplasia Cutis Congenita-Epibulbar Dermoids Syndrome
|
Oculo-Ectodermal Syndrome
|
|
Toriello Lacassie Droste Syndrome
|
|
|
| Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
|
Charcot-Marie-Tooth Disease Type 4
|
Charcot-Marie-Tooth Disease Type 4e
|
|
Hereditary Motor And Sensory Neuropathy
|
Cmt4e
|
|
CHN1
|
Hypomyelinating Neuropathy, Congenital, 1
|
|
Charcot-Marie-Tooth Neuropathy Type 4e
|
Neuropathy, Congenital Hypomyelinating, 1
|
|
Ar-Cmt1
|
Autosomal Recessive Demyelinating Charcot-Marie-Tooth
|
|
Cmt4
|
Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive
|
|
Hypomyelination, Severe Congenital
|
Charcot-Marie-Tooth Disease, Type 4e
|
|
Charcot-Marie-Tooth Neuropathy, Type 4e
|
Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy
|
|
Autosomal Recessive Congenital Hypomyelinating Neuropathy
|
Congenital Amyelinating Neuropathy
|
|
Congenital Hypomyelinating Neuropathy Autosomal Recessive
|
Neuropathy, Congenital Hypomyelinating Or Amyelinating
|
|
Severe Congenital Hypomyelination
|
Hereditary Sensory Motor Neuropathy
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive
|
Neuropathy, Hypomyelinating, Congenital, Type 1
|
|
Neuropathy, Motor And Sensory, Hereditary
|
Congenital Hypomyelinating Neuropathy
|
|
Hereditary Motor And Sensory Neuropathies
|
Hereditary Sensorimotor Neuropathy
|
|
Hmsn - [Hereditary Motor And Sensory Neuropathy]
|
Hsmn - [Hereditary Sensory And Motor Neuropathy]
|
|
Hereditary Motor And Sensory Neuropathy, Types I-Iv
|
|
|
| Charcot-Marie-Tooth Disease And Deafness |
|
Charcot-Marie-Tooth Disease Type 1e
|
CMT1E
|
|
Charcot-Marie-Tooth Disease Type 1
|
Hereditary Motor And Sensory Neuropathy Type 1
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
|
Charcot-Marie-Tooth Disease, Type I
|
|
Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant
|
Charcot-Marie-Tooth Disease, Type 1e
|
|
Charcot-Marie-Tooth Disease Demyelinating Type 1e
|
Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease
|
|
Cmt1
|
Charcot-Marie-Tooth Neuropathy Type 1
|
|
Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness
|
Charcot-Marie-Tooth Disease-Deafness
|
|
Charcot-Marie-Tooth Type 1
|
Hmsn1
|
|
Hereditary Motor And Sensory Neuropathy 1
|
Cmt 1e
|
|
Charcot Marie Tooth Disease Type 1e
|
Charcot-Marie-Tooth Disease-Deafness Syndrome
|
|
Charcot-Marie-Tooth Disease-Hearing Loss Syndrome
|
Charcot-Marie-Tooth Disease 1e
|
|
Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant
|
Charcot-Marie-Tooth Neuropathy Type 1e
|
|
Charcot-Marie-Tooth Disease, Type Ie
|
Hereditary Motor And Sensory Neuropathy Type I
|
|
|
| Scoliosis |
|
|
| Presbyopia |
|
Subnormal Accommodation
|
Accommodation Insufficiency Of Old Age
|
|
|
| Pseudohypoaldosteronism, Type I, Autosomal Recessive |
|
Autosomal Recessive Pseudohypoaldosteronism Type 1
|
PHA1B
|
|
Pseudohypoaldosteronism Type 1
|
Pseudohypoaldosteronism, Type I
|
|
Generalized Pha1
|
Generalized Pseudohypoaldosteronism Type 1
|
|
Pseudohypoaldosteronism Type 1 Autosomal Recessive
|
Pha1
|
|
Pseudohypoaldosteronism
|
Pha I, Autosomal Recessive
|
|
Autosomal Recessive Pha 1
|
Pseudohypoaldosteronism Type 1, Recessive
|
|
Pseudohypoaldosteronism Type I
|
Autosomal Recessive Pha1
|
|
Pha Type 1
|
Pseudohypoaldosteronism 1, Autosomal Recessive
|
|
Multisystem Pseudohypoaldosteronism
|
Pha Type I, Autosomal Recessive
|
|
Pseudohypoaldosteronism Type I, Autosomal Recessive
|
|
|
| Acute Cystitis |
|
Urinary Tract Infection
|
Recurrent Urinary Tract Infection
|
|
|
| Interstitial Cystitis |
|
Bladder Pain Syndrome
|
Painful Bladder Syndrome
|
|
Ulcerative Cystitis
|
Ic/Bps
|
|
Ic/Pbs
|
Interstitial Cystitis/Bladder Pain Syndrome
|
|
Interstitial Cystitis/Painful Bladder Syndrome
|
Cystitis, Interstitial
|
|
Chronic Interstitial Cystitis
|
Pelvic Congestion Syndrome
|
|
Trigonitis
|
|
|
| Mucolipidosis Iv |
|
Mucolipidosis Type Iv
|
ML4
|
|
Sialolipidosis
|
Mucolipidosis Type 4
|
|
Ganglioside Sialidase Deficiency
|
Mliv
|
|
Ml Iv
|
Berman Syndrome
|
|
Ganglioside Neuraminidase Deficiency
|
Ml 4
|
|
Mucolipidosis 4
|
Type Iv Mucolipidosis
|
|
Gangliosidoses
|
|
|
| Spastic Paraplegia 76, Autosomal Recessive |
|
SPG76
|
Autosomal Recessive Spastic Paraplegia Type 76
|
|
Hereditary Spastic Paraplegia 76
|
Autosomal Recessive Spastic Paraplegia 76
|
|
Paraplegia, Spastic, Autosomal Recessive, Type 76
|
|
|
| Somatoform Disorder |
|
Physiological Malfunction Arising From Mental Factor
|
Psychosomatic Disorder
|
|
Psychophysiologic Disorders
|
|
|
| Paine Syndrome |
|
Pain Disorder
|
Pain
|
|
Microcephaly With Spastic Diplegia
|
Pain Syndrome
|
|
|
| Bone Development Disease |
|
|
| Cerebral Cavernous Malformations |
|
Cerebral Cavernous Malformation
|
Cavernous Malformations Of Cns And Retina
|
|
Cerebral Cavernous Malformation 1
|
Cavernous Angiomatous Malformations
|
|
Cerebral Capillary Malformations
|
CCM
|
|
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations
|
Familial Cavernous Angioma
|
|
Cavernous Angioma
|
Familial Cerebral Cavernous Malformation
|
|
Cerebral Cavernous Malformations 1
|
Cavernous Angioma, Familial
|
|
Cam
|
Cerebral Cavernous Malformations-1
|
|
Cavernoma
|
Central Nervous System Cavernous Hemangioma
|
|
Cerebral Cavernous Hemangioma
|
Familial Cavernous Hemangioma
|
|
Familial Cavernous Malformation
|
Familial Cerebral Cavernous Angioma
|
|
Intracerebral Cavernous Hemangioma
|
CCM1
|
|
Cavernous Hemangioma Of The Brain
|
Cerebral Cavernoma
|
|
Cerebral Cavernous Malformations, Type 1
|
Hemangioma, Cavernous, Central Nervous System
|
|
Hemangioma, Cavernous
|
Angioma, Cavernous
|
|
|
| Erythromelalgia |
|
Primary Erythromelalgia
|
Erythermalgia
|
|
Primary Erythermalgia
|
Mitchell Disease
|
|
Familial Erythromelalgia
|
|
|
| Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
|
Dehydrated Hereditary Stomatocytosis
|
Hereditary Xerocytosis
|
|
Xerocytosis, Hereditary
|
Pshk1
|
|
Pseudohyperkalemia Edinburgh
|
Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema
|
|
DHS1
|
Dhs
|
|
Hereditary Desiccytosis
|
Dehydrated Hereditary Stomatocytosis 1
|
|
Desiccytosis, Hereditary
|
Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak
|
|
Pseudohyperkalemia Familial 1, Due To Red Cell Leak
|
Desiccytosis Hereditary
|
|
Xerocytosis Hereditary
|
Familial Pseudohyperkalemia 1 Due To Red Cell Leak
|
|
Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema
|
Xerocytosis
|
|
|
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Autosomal Recessive Polycystic Kidney Disease
|
Arpkd
|
|
Polycystic Kidney Disease, Autosomal Recessive
|
Polycystic Kidney And Hepatic Disease 1
|
|
Pkhd1
|
PKD4
|
|
Polycystic Kidney Disease 4 With Or Without Hepatic Disease
|
Polycystic Kidney Disease, Infantile, Type I
|
|
Polycystic Kidney Disease, Infantile Type
|
Polycystic Kidney, Autosomal Recessive
|
|
Pkd3, Formerly
|
Polycystic Kidney Disease 4, With Or Without Hepatic Disease
|
|
Arpkd/Chf
|
Ar-Pkd
|
|
Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease
|
Infantile Polycystic Kidney Disease Type I
|
|
Pkd3
|
Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease
|
|
Polycystic Kidney Disease 3, Autosomal Dominant
|
|
|
| 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]
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Hypertrophic Neuropathy Of Dejerine-Sottas |
|
Dejerine-Sottas Disease
|
Dejerine-Sottas Syndrome
|
|
Charcot-Marie-Tooth Disease Type 3
|
DSS
|
|
Hereditary Motor And Sensory Neuropathy Type Iii
|
Hmsn3
|
|
Dejerine-Sottas Neuropathy
|
Hmsn Iii
|
|
Charcot-Marie-Tooth Disease, Type 3
|
Cmt3
|
|
Dsn
|
Hmsn 3
|
|
Hereditary Motor And Sensory Neuropathy Type 3
|
Hereditary Motor And Sensory Neuropathy 3
|
|
Hypertrophic Neuropathy Of Infancy
|
Charcot-Marie-Tooth Disease Demyelinating Type 4f
|
|
Charcot-Marie-Tooth Disease Type 4f
|
Charcot-Marie-Tooth Neuropathy Type 4f
|
|
Cmt4f
|
Hereditary Motor And Sensory Neuropathy Iii
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
|
|
|
| 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
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| 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
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
