Diseases |
Alias |
|
Paraganglioma And Gastric Stromal Sarcoma |
Carney-Stratakis Syndrome
|
Paraganglioma And Gastrointestinal Stromal Tumor
|
Carney Dyad
|
Carney-Stratakis Dyad Of Paraganglioma And Gastric Stromal Sarcoma
|
Paraganglioma And Gist
|
Carney-Stratakis Dyad
|
Gist-Paraganglioma Dyad
|
PGGSS
|
Paraganglioma, Gastric Stromal Sarcoma
|
Gastrointestinal Stromal Tumors
|
|
|
Paragangliomas 1 |
Carotid Body Tumor
|
Paragangliomata
|
Pgl
|
Chemodectomas
|
Carotid Body Tumors
|
Glomus Jugulare Tumors
|
Carotid Body Paraganglioma
|
PGL1
|
Cbt1
|
Glomus Tumor
|
Glomus Tumors Familial 1
|
Paragangliomas Familial 1
|
Glomus Jugulare Tumor
|
Paragangliomas, Familial, 1
|
Glomus Tumors, Familial, 1
|
Paraganglioma, Carotid Body
|
Paragangliomas, Familial Nonchromaffin, 1
|
Paragangliomas 1, With Or Without Deafness
|
Cbt
|
Paraganglioma - Glomus Jugulare
|
Pgl 1
|
Sdhd-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
Chemodectoma
|
Familial Non-Chromaffin Paragangliomas 1
|
Familial Paragangliomas Non-Chromaffin 1 With Or Without Deafness
|
Paraganglioma Carotid Body
|
Paragangliomas, Type 1
|
Paraganglioma
|
Extra-Adrenal Paraganglioma
|
Glomus Tympanicum Tumor
|
|
|
Mitochondrial Complex Iii Deficiency, Nuclear Type 2 |
Mitochondrial Complex Iii Deficiency Nuclear Type 2
|
MC3DN2
|
Mitochondrial Complex Ii Deficiency, Nuclear Type 3
|
MC2DN3
|
Mitochondrial Complex 2 Deficiency, Nuclear Type 3
|
Mitochondrial Complex Iii Deficiency, Nuclear 2
|
|
|
Mitochondrial Complex Ii Deficiency |
Isolated Mitochondrial Respiratory Chain Complex Ii Deficiency
|
Isolated Succinate-Coenzyme Q Reductase Deficiency
|
Isolated Succinate-Coq Reductase Deficiency
|
Isolated Succinate-Ubiquinone Reductase Deficiency
|
Mitochondrial Respiratory Chain Complex Ii Deficiency
|
Complex 2 Mitochondrial Respiratory Chain Deficiency
|
Succinate Coq Reductase Deficiency
|
Succinate Dehydrogenase Deficiency
|
Isolated Succinate Dehydrogenase Deficiency
|
Succinate-Coenzyme Q Reductase Deficiency
|
|
|
Pheochromocytoma |
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
PCC
|
Chromaffin Cell Tumor
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
Pheochromoblastoma
|
Pheochromocytomas
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
Cowden Syndrome |
Cowden Disease
|
Multiple Hamartoma Syndrome
|
Cowden'S Disease
|
Lhermitte-Duclos Disease
|
Cd
|
Cs
|
Mham
|
Dysplastic Gangliocytoma Of Cerebellum
|
Cowden'S Syndrome
|
Hamartoma Syndrome, Multiple
|
|
|
Hereditary Paraganglioma-Pheochromocytoma Syndromes |
Hereditary Pheochromocytoma-Paraganglioma
|
Hereditary Paraganglioma-Pheochromocytoma
|
Familial Pheochromocytoma-Paraganglioma
|
Paragangliomas 2
|
Paragangliomas 3
|
Paragangliomas 4
|
Sdhx-Related Paraganglioma-Pheochromocytoma
|
Familial Paraganglioma Syndrome
|
Familial Paraganglioma-Pheochromocytoma Syndromes
|
Fpgl
|
Fpgl/Pheo
|
Paragangliomas 1
|
Paraganglioma
|
|
|
Paraganglioma |
Chemodectoma
|
Glomus Body Tumor
|
Paragangliomas
|
Carotid Body Paraganglioma
|
Extra-Adrenal Paraganglioma
|
|
|
Mitochondrial Complex Ii Deficiency, Nuclear Type 1 |
MC1DN2
|
MC2DN1
|
Succinate Coq Reductase Deficiency
|
Succinate Dehydrogenase Deficiency
|
Mitochondrial Complex I Deficiency, Nuclear Type 2
|
Mitochondrial Complex 1 Deficiency, Nuclear Type 2
|
Nuclear Type Mitochondrial Complex I Deficiency 2
|
Complex 2 Mitochondrial Respiratory Chain Deficiency
|
Complex Ii Mitochondrial Respiratory Chain Deficiency
|
Sdh-Defective Infantile Leukoencephalopathy
|
|
|
Cowden Syndrome 1 |
Bannayan-Riley-Ruvalcaba Syndrome
|
Pten Hamartoma Tumor Syndrome
|
Lhermitte-Duclos Disease
|
Bannayan-Zonana Syndrome
|
Phts
|
Riley-Smith Syndrome
|
Bzs
|
Ruvalcaba-Myhre-Smith Syndrome
|
Multiple Hamartoma Syndrome
|
Rmss
|
Brrs
|
Dysplastic Gangliocytoma Of The Cerebellum
|
CWS1
|
Cs
|
Cd
|
Mham
|
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
|
Macrocephaly Multiple Lipomas And Hemangiomata
|
Bannayan-Ruvalcaba-Riley Syndrome
|
Myhre-Riley-Smith Syndrome
|
LDD
|
Cerebelloparenchymal Disorder Vi
|
Hamartoma Syndrome, Multiple
|
Bbrs
|
Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata
|
Macrocephaly, Multiple Lipomas, And Hemangiomata
|
Macrocephaly Pseudopapilledema And Multiple Hemangiomas
|
Ruvalcaba -Myhre-Smith Syndrome
|
Ruvalcaba-Myhre Syndrome
|
Cowden Disease
|
Macrocephaly Pseudopapilledema And Multiple Hemangiomata
|
Cerebellar Granule Cell Hypertrophy And Megalencephaly
|
Cpd6
|
Pten Hamartoma Tumor Syndromes
|
Cowden Syndrome, Type 1
|
|
|
Bap1 Tumor Predisposition Syndrome |
Bap1-Related Tumor Predisposition Syndrome
|
Common Syndrome
|
Bap1 Cancer Syndrome
|
Bap1-Tpds
|
Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms
|
Tumor Predisposition Syndrome
|
Tumor Susceptibility Linked To Germline Bap1 Mutations
|
Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms
|
Tumor Predisposition
|
|
|
Inherited Cancer-Predisposing Syndrome |
Hereditary Cancer-Predisposing Syndrome
|
|
|
Carcinoid Syndrome |
Carcinoid Tumor
|
Malignant Carcinoid Syndrome
|
Carcinoid Tumor Syndrome
|
Carcinoid Tumors
|
Carcinoid Tumor No Icd-O Subtype
|
Argentaffinoma Syndrome
|
|
|
Glomus Tumor |
Glomus Neoplasm
|
Glomus Tumour
|
|
|
Chondroma |
Central Chondroma
|
Enchondroma
|
|
|
Neurofibromatosis |
Neurofibromatoses
|
Acoustic Neurofibromatosis
|
Central Neurofibromatosis
|
Peripheral Neurofibromatosis
|
Recklinghausen'S Neurofibromatosis
|
Von Reklinghausen Disease
|
Neurofibromatosis Type 1
|
|
|
Von Hippel-Lindau Syndrome |
Von Hippel-Lindau Disease
|
Vhl
|
Vhl Syndrome
|
VHLS
|
Von Hippel-Lindau Syndrome, Modifier Of
|
Hippel Lindau Syndrome
|
Angiomatosis Retinae
|
Cerebelloretinal Angiomatosis, Familial
|
Hippel-Lindau Disease
|
Familial Cerebelloretinal Angiomatosis
|
Lindau Disease
|
VHLD
|
|
|
Sporadic Pheochromocytoma/Secreting Paraganglioma |
|
|
Persistent Generalized Lymphadenopathy |
Pgl
|
Persistant Generalized Lymphadenopathy
|
|
|
Extra-Adrenal Pheochromocytoma |
Pheochromocytoma, Extra-Adrenal
|
|
|
Carney Triad |
Gastric Leiomyosarcoma, Pulmonary Chondroma, And Extraadrenal Paraganglioma
|
|
|
Gastric Leiomyosarcoma |
Leiomyosarcoma Of Stomach
|
|
|
Neurofibromatosis, Type I |
Von Recklinghausen Disease
|
Neurofibromatosis 1
|
Neurofibromatosis, Type 1
|
NF1
|
Neurofibromatosis, Peripheral Type
|
Neurofibromatosis Type I
|
Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion
|
Familial Spinal Neurofibromatosis
|
Fsnf
|
Peripheral Neurofibromatosis
|
Von Recklinghausen'S Neurofibromatosis
|
Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion
|
Neurofibromatosis Peripheral Type
|
Von Recklinghausen Syndrome
|
Neurofibromatosis Type 1
|
Von Recklinghausen Neuropathy
|
Nf1 - [Neurofibromatosis Type 1]
|
Recklinghausen Disease
|
|
|
Multiple Endocrine Neoplasia, Type Iia |
Multiple Endocrine Neoplasia Type 2a
|
Sipple Syndrome
|
Multiple Endocrine Neoplasia Type 2
|
MEN2A
|
Men2
|
Ptc Syndrome
|
Multiple Endocrine Neoplasia, Type 2
|
Multiple Endocrine Neoplasia Iia
|
Men 2a
|
Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma
|
Multiple Endocrine Neoplasia, Type 2a
|
Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma
|
Multiple Endocrine Neoplasia Ii
|
Men2 Syndrome
|
Men-2a Syndrome
|
Multiple Neoplasia 2a
|
Multiple Neoplasia Type 2
|
|
|
Malignant Pheochromocytoma |
Pheochromocytoma, Malignant
|
|
|
Adrenal Medulla Cancer |
Adrenal Medulla Neoplasm
|
Adrenal Medulla Tumor
|
Malignant Neoplasm Of Adrenal Medulla
|
Malignant Tumor Of The Adrenal Medulla
|
Adrenal Medulla Carcinoma
|
Neoplasm Of Adrenal Medulla
|
|
|
Lymph Node Disease |
Abnormality Of The Lymph Nodes
|
Disorder Of Lymph Node
|
|
|
Kearns-Sayre Syndrome |
Ophthalmoplegia
|
Mitochondrial Cytopathy
|
KSS
|
Ophthalmoplegia, Pigmentary Degeneration Of Retina, And Cardiomyopathy
|
Oculocraniosomatic Syndrome
|
Chronic Progressive External Ophthalmoplegia With Myopathy
|
Cpeo With Myopathy
|
Total Ophthalmoplegia
|
Ophthalmoplegia-Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers
|
Cpeo With Ragged-Red Fibers
|
Oculomotor Paralysis
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication O
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication Of Mitochondrial Dna
|
Proximal Tubulopathy, Diabetes Mellitus And Cerebellar Ataxia
|
Cpeo With Ragged Red Fibers
|
Ophthalmoplegia Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged Red Fibers
|
Kearns-Sayre Mitochondrial Cytopathy
|
Mitochondrial Myopathies
|
|
|
Multiple Endocrine Neoplasia |
Men
|
Multiple Endocrine Adenomatosis
|
Multiple Endocrine Neoplasia Syndrome
|
Adenomatosis, Familial Endocrine
|
Endocrine Neoplasia, Multiple
|
Familial Endocrine Adenomatosis
|
Mea
|
Multiple Endocrine Neoplasms
|
Multiple Endocrine Neoplasia Type 1
|
|
|
Neural Crest Tumor |
Neural Crest-Derived Tumors
|
|
|
Leprosy 3 |
Leprosy
|
Leprosy, Susceptibility To, 3
|
Hansen'S Disease
|
Leprosy, Susceptibility To
|
Hansen Disease
|
Infection Due To Mycobacterium Leprae
|
LPRS3
|
Leprosy, Type 3
|
Anaesthesia Leprosy
|
Anaesthetic Leprosy
|
Maculoanaesthetic Leprosy
|
Macular Leprosy
|
Leprosy Unspecified
|
|
|
Endocrine Organ Benign Neoplasm |
|
|
Indeterminate Leprosy |
|
|
Multiple Endocrine Neoplasia, Type I |
Multiple Endocrine Neoplasia Type 1
|
MEN1
|
Wermer Syndrome
|
Multiple Endocrine Neoplasia 1
|
Multiple Endocrine Neoplasia, Type 1
|
Men I
|
Endocrine Adenomatosis, Multiple
|
Mea I
|
Men Type I
|
Wermer'S Syndrome
|
Men1 Syndrome
|
Multiple Endocrine Adenomatosis
|
Endocrine Adenomatosis Multiple
|
Men 1
|
Familial Multiple Endocrine Neoplasia Type I
|
Neoplasia, Endocrine, Multiple, Type 1
|
Multiple Endocrine Neoplasia
|
|
|
Neuroendocrine Tumor |
Neuroendocrine Neoplasm
|
Neuroendocrine Tumors
|
Carcinoma, Neuroendocrine
|
|
|
Quadriplegia |
|
|
Acoustic Neuroma |
Neurofibromatosis Type 2
|
Vestibular Schwannoma
|
Acoustic Neurinoma
|
Bilateral Acoustic Neurofibromatosis
|
Nf2
|
Acoustic Neurilemoma
|
Cerebellopontine Angle Tumor
|
Neurofibromatosis Central Type
|
Neurofibromatosis Type Ii
|
Vestibular Neurilemmoma
|
Acoustic Tumor
|
Neurinoma Of The Acoustic Nerve
|
Acoustic Neurinoma Bilateral
|
Acoustic Schwannomas Bilateral
|
Banf
|
Central Neurofibromatosis
|
Familial Acoustic Neuromas
|
Neurofibromatosis 2
|
Neurofibromatosis Type 2 Merlin
|
Schwannoma, Acoustic, Bilateral
|
Neuroma Acoustic
|
Neuroma, Acoustic
|
Familial Acoustic Neuroma
|
Familial Vestibular Schwannoma
|
Neurofibromatosis, Central Type
|
Nf2 - [Neurofibromatosis Type 2]
|
|
|
Leiomyoma Cutis |
Cutaneous Leiomyoma
|
Leiomyoma Of The Skin
|
|
|
Dermis Tumor |
Dermis Tumour
|
Neoplasm Of Dermis
|
Tumor Of Dermis
|
Tumour Of Dermis
|
|
|
Carotid Body Cancer |
Cancer Of Carotid Body
|
Malignant Carotid Body Paraganglioma
|
Malignant Carotid Body Tumor
|
Malignant Neoplasm Of Carotid Body
|
|
|
Tuberculoid Leprosy |
Smooth Leprosy
|
Type T Leprosy
|
Leprosy Tuberculoid
|
Leprosy, Tuberculoid
|
|
|
Mobitz Type Ii Atrioventricular Block |
Mobitz Ii Atrioventricular Block
|
Mobitz Ii Atrioventricular Block
|
|
|
Borderline Leprosy |
Midborderline Leprosy
|
Borderline Or Dimorphous Leprosy
|
Leprosy, Borderline
|
|
|
Scrotum Melanoma |
|
|
Adrenal Cortical Adenoma |
Adrenocortical Adenoma
|
Adenoma Adrenocortical
|
|
|
Foster-Kennedy Syndrome |
Disorder Of The Optic Nerve
|
Optic Nerve Diseases
|
Disease Of Optic Cranial Nerve
|
Disease Of Optic Nerve
|
Disease Of Second Cranial Nerve
|
Disorder Of Optic Cranial Nerve
|
Disorder Of Second Cranial Nerve
|
Disorders Of 2nd Nerve
|
|
|
Cerebral Angioma |
Hemangioma Of Cerebrum
|
Cerebral Hemangioma
|
|
|
Horner'S Syndrome |
Horner Syndrome
|
Bernard-Horner Syndrome
|
Oculosympathetic Palsy
|
Bernard Horner Syndrome
|
Cervical Sympathetic Paralysis
|
Von Passow Syndrome
|
Cervical Sympathetic Dystrophy
|
|
|
Multiple Endocrine Neoplasia, Type Iib |
Multiple Endocrine Neoplasia Type 2b
|
MEN2B
|
Wagenmann-Froboese Syndrome
|
Multiple Endocrine Neoplasia Iib
|
Mucosal Neuroma Syndrome
|
Multiple Endocrine Neoplasia, Type 3
|
Multiple Endocrine Neoplasia, Type 2b
|
Men Iib
|
Neuromata, Mucosal, With Endocrine Tumors
|
Multiple Endocrine Neoplasia, Type Iii, Formerly
|
Men3, Formerly
|
Men Type Iib
|
Men 2b
|
Multiple Endocrine Neoplasia Type 3
|
Multiple Neoplasia 2b
|
Neoplasia, Endocrine, Multiple, Type Iib
|
|
|
Peripheral Nervous System Benign Neoplasm |
|
|
Autonomic Nervous System Benign Neoplasm |
|
|
Spastic Quadriplegia |
Spastic Quadriplegic Cerebral Palsy
|
Quadriplegic Infantile Cerebral Palsy
|
Tetraplegic Infantile Cerebral Palsy
|
Cerebral Palsy Spastic Quadriplegic
|
Quadriplegic Cerebral Palsy
|
Spastic Quadriplegia Cerebral Palsy
|
Spastic Tetraplegia Cerebral Palsy
|
Cerebral Palsy, Quadriplegic, Infantile
|
Cerebral Palsy With Spastic Tetraplegia
|
Congenital Spastic Quadriplegia
|
Spastic Tetraplegic Cerebral Palsy
|
Congenital Quadriplegia Nos
|
Tetraplegic Cerebral Palsy
|
|
|
Adrenal Carcinoma |
Adrenal Cancer
|
Adrenal Gland Cancer
|
Malignant Neoplasm Of Adrenal Gland
|
Adrenal Gland Neoplasms
|
Carcinoma Of The Adrenal Gland
|
Adrenal Neoplasm
|
Malignant Adrenal Tumor
|
Neoplasm Of Adrenal Gland
|
Tumor Of The Adrenal Gland
|
Adrenal Gland Neoplasm
|
Adrenocortical Carcinoma
|
Adrenal Gland Malignancy
|
Suprarenal Cancer
|
Malignant Neoplasm Of Suprarenal Gland
|
Malignant Neoplasm Of Adrenal Gland, Unspecified
|
Malignant Tumour Of Adrenal Gland
|
Suprarenal Gland Cancer
|
Primary Malignant Neoplasm Of Adrenal Gland
|
|
|
Leigh Syndrome |
Leigh Disease
|
Infantile Subacute Necrotizing Encephalopathy
|
Leigh Syndrome Due To Mitochondrial Complex Iv Deficiency
|
LS
|
Sne
|
Leigh'S Disease
|
Leigh Syndrome Due To Mitochondrial Complex I Deficiency
|
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh
|
Subacute Necrotizing Encephalomyelopathy
|
Necrotizing Encephalopathy Infantile Subacute Of Leigh
|
Leigh Syndrome Due To Mitochondrial Complex Iii Deficiency
|
Infantile Necrotizing Encephalomyelopathy
|
Juvenile Subacute Necrotizing Encephalomyelopathy
|
Leigh'S Necrotizing Encephalopathy
|
Subacute Necrotizing Encephalopathy
|
Juvenile Subacute Necrotizing Encephalopathy
|
Leigh Syndrome Due To Mitochondrial Complex Ii Deficiency
|
Leigh Syndrome Due To Mitochondrial Complex V Deficiency
|
Encephalopathy, Subacute Necrotizing, Infantile
|
Encephalopathy, Subacute Necrotizing, Juvenile
|
Maternally Inherited Leigh Syndrome
|
Subacute Necrotising Encephalomyelopathy
|
Subacute Necrotising Encephalopathy
|
|
|
Lepromatous Leprosy |
Leprosy, Lepromatous
|
Type L Leprosy
|
Leprosy Lepromatous
|
|
|
Cranial Nerve Palsy |
Cranial Nerve Paralysis
|
Cranial Nerve Diseases
|
Cranial Nerve Palsies
|
|
|
Hereditary Renal Cell Carcinoma |
|
|
Cardiovascular Organ Benign Neoplasm |
|
|
Fumarase Deficiency |
Fumaric Aciduria
|
FMRD
|
Fumarate Hydratase Deficiency
|
Deficiency, Fumarase
|
|
|
Thyroid Gland Cancer |
Thyroid Gland Carcinoma
|
Malignant Neoplasm Of Thyroid Gland
|
Malignant Tumour Of Thyroid Gland
|
Thyroid Neoplasm
|
Thyroid Neoplasms
|
Neoplasm Of Thyroid Gland
|
Thyroid Gland Neoplasm
|
Head And Neck Cancer, Thyroid
|
Neoplasm Of The Thyroid Gland
|
Cancer Of The Thyroid
|
Primary Malignant Neoplasm Of Thyroglossal Duct
|
Malignant Neoplasm Of Thyroglossal Duct
|
Primary Malignant Neoplasm Of Thyroid Gland
|
Thyroglossal Duct Cancer
|
Toxic Goitre Malignant Tumour
|
Cancerous Goitre
|
|
|
Renal Oncocytoma |
Oncocytoma, Renal
|
Oncocytoma Of Kidney
|
Renal Epithelial Oncocytic Tumor
|
Oncocytoma Kidney
|
Oncocytoma Renal
|
Kidney Oncocytoma
|
|
|
Gastrointestinal Stromal Tumor |
GIST
|
Gastrointestinal Stromal Tumors
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
Gant
|
Gastrointestinal Stromal Tumour
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
Plexosarcoma
|
|
|
Gastric Liposarcoma |
Liposarcoma Of The Stomach
|
|
|
Carney Complex Variant |
Carney Complex
|
Carney Syndrome
|
Carney Complex, Type 1
|
Lamb Syndrome
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
Car
|
Cnc1
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
CACOV
|
|
|
Dystonia |
Dystonic Disease
|
Dystonic Disorder
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|