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Hajdu-Cheney Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Biological Phenomena, Cell Phenomena, and Immunity ∟ Biological Phenomena ∟ Regeneration ∟ Bone Remodeling ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal, Neural, and Ocular Physiology ∟ Musculoskeletal Physiology ∟ Musculoskeletal Physiologic Processes ∟ Bone Remodeling ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome 42 coordinate concepts ∟ Arthrogryposis \| ∟ Craniofacial Abnormalities \| ∟ Funnel Chest \| ∟ Gastroschisis \| ∟ Hip Dislocation, Congenital \| ∟ Klippel-Feil Syndrome \| ∟ Limb Deformities, Congenital \| ∟ Synostosis \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Eye Diseases, Hereditary \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Biological Phenomena, Cell Phenomena, and Immunity ∟ Biological Phenomena ∟ Regeneration ∟ Bone Remodeling ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Musculoskeletal Abnormalities ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Musculoskeletal Abnormalities ∟ Hajdu-Cheney Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal, Neural, and Ocular Physiology ∟ Musculoskeletal Physiology ∟ Musculoskeletal Physiologic Processes ∟ Bone Remodeling ∟ Bone Resorption ∟ Osteolysis ∟ Acro-Osteolysis ∟ Hajdu-Cheney Syndrome Acro-Osteolysis > Osteolysis > Bone Resorption > Bone Remodeling > Regeneration > Biological Phenomena > Biological Phenomena, Cell Phenomena, and Immunity > Medical Subject Headings (MeSH) Musculoskeletal Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Acro-Osteolysis > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Acro-Osteolysis > Osteolysis > Bone Resorption > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Musculoskeletal Abnormalities > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Acro-Osteolysis > Osteolysis > Bone Resorption > Bone Remodeling > Musculoskeletal Physiologic Processes > Musculoskeletal Physiology > Musculoskeletal, Neural, and Ocular Physiology > Medical Subject Headings (MeSH) X
History note:	Bone Diseases, Developmental (1973-1984) \| Osteolysis (1976-1986) \| Osteolysis, Essential (1980-2002)X
historyNote*:	2003; use OSTEOLYSIS, ESSENTIAL 1987-2002 X
publicMeSHNote*:	2003; see OSTEOLYSIS, ESSENTIAL 1987-2002 X
Scope note:	Rare, autosomal dominant syndrome characterized by ACRO-OSTEOLYSIS, generalized OSTEOPOROSIS, and skull deformations. X
activeMeSHYear*:	2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	2002-07-03X
dateEstablished*:	2003-01-01X
Type:	Concept X
Coordinate terms:	Arthrogryposis \| Craniofacial Abnormalities \| Funnel Chest \| Gastroschisis \| Hip Dislocation, Congenital \| Klippel-Feil Syndrome \| Limb Deformities, Congenital \| Synostosis \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| CADASIL \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Eye Diseases, Hereditary \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Hajdu-Cheneyn oireyhtymä (fi) Hajdu-Cheneyn syndrooma (fi, replaced) Hajdu-Cheneys syndrom (sv) Idiopatisk osteolys typ 6 (sv, replaced) Osteolysis, Multicentric (en, replaced) X
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