ONKI3 | Medical Subject Headings

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Cri-du-Chat Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome 37 coordinate concepts ∟ D008607Q000193* \| ∟ De Lange Syndrome \| ∟ Down Syndrome \| ∟ Mental Retardation, X-Linked \| ∟ Prader-Willi Syndrome \| ∟ Rubinstein-Taybi Syndrome \| ∟ WAGR Syndrome \| ∟ Williams Syndrome \| ∟ Angelman Syndrome \| ∟ Beckwith-Wiedemann Syndrome \| ∟ Branchio-Oto-Renal Syndrome \| ∟ Holoprosencephaly \| ∟ Sex Chromosome Disorders \| ∟ Alagille Syndrome \| ∟ Bardet-Biedl Syndrome \| ∟ Basal Cell Nevus Syndrome \| ∟ Bloom Syndrome \| ∟ Cockayne Syndrome \| ∟ Ectodermal Dysplasia \| ∟ Gardner Syndrome \| ∟ Incontinentia Pigmenti \| ∟ Laurence-Moon Syndrome \| ∟ LEOPARD Syndrome \| ∟ Marfan Syndrome \| ∟ Mobius Syndrome \| ∟ Nail-Patella Syndrome \| ∟ Oculocerebrorenal Syndrome \| ∟ Orofaciodigital Syndromes \| ∟ POEMS Syndrome \| ∟ Proteus Syndrome \| ∟ Prune Belly Syndrome \| ∟ Rubella Syndrome, Congenital \| ∟ Short Rib-Polydactyly Syndrome \| ∟ Smith-Lemli-Opitz Syndrome \| ∟ Waardenburg's Syndrome \| ∟ Wolfram Syndrome \| ∟ Zellweger Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Behavior and Behavior Mechanisms ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Chromosome Disorders ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Chromosome Disorders ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Mental Disorders ∟ Mental Disorders Diagnosed in Childhood ∟ Mental Retardation ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome Medical Subject Headings (MeSH) ∟ Pathological Conditions, Signs and Symptoms ∟ Signs and Symptoms ∟ Neurologic Manifestations ∟ Neurobehavioral Manifestations ∟ Mental Retardation ∟ Cri-du-Chat Syndrome Mental Retardation > Neurobehavioral Manifestations > Behavior and Behavior Mechanisms > Medical Subject Headings (MeSH) Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Chromosome Disorders > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Chromosome Disorders > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Mental Retardation > Mental Disorders Diagnosed in Childhood > Mental Disorders > Medical Subject Headings (MeSH) Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Nervous System Diseases > Medical Subject Headings (MeSH) Mental Retardation > Neurobehavioral Manifestations > Neurologic Manifestations > Signs and Symptoms > Pathological Conditions, Signs and Symptoms > Medical Subject Headings (MeSH) X
historyNote*:	77; was CRYING CAT SYNDROME 1964-76 X
onlineNote*:	use CRI-DU-CHAT SYNDROME to search CRYING CAT SYNDROME 1966-76 X
publicMeSHNote*:	77; was CRYING CAT SYNDROME 1964-76 X
Scope note:	An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-). X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1966-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Mental Retardation X
Type:	Concept X
Coordinate terms:	D008607Q000193* \| De Lange Syndrome \| Down Syndrome \| Mental Retardation, X-Linked \| Prader-Willi Syndrome \| Rubinstein-Taybi Syndrome \| WAGR Syndrome \| Williams Syndrome \| Angelman Syndrome \| Beckwith-Wiedemann Syndrome \| Branchio-Oto-Renal Syndrome \| Holoprosencephaly \| Sex Chromosome Disorders \| Alagille Syndrome \| Bardet-Biedl Syndrome \| Basal Cell Nevus Syndrome \| Bloom Syndrome \| Cockayne Syndrome \| Ectodermal Dysplasia \| Gardner Syndrome \| Incontinentia Pigmenti \| Laurence-Moon Syndrome \| LEOPARD Syndrome \| Marfan Syndrome \| Mobius Syndrome \| Nail-Patella Syndrome \| Oculocerebrorenal Syndrome \| Orofaciodigital Syndromes \| POEMS Syndrome \| Proteus Syndrome \| Prune Belly Syndrome \| Rubella Syndrome, Congenital \| Short Rib-Polydactyly Syndrome \| Smith-Lemli-Opitz Syndrome \| Waardenburg's Syndrome \| Wolfram Syndrome \| Zellweger Syndrome X
URI:	X
Labels and equivalent concepts:	Kissanhuuto-oireyhtymä (fi) Kissanhuuto-syndrooma (fi, replaced) Cri-du-chat -syndrooma (fi, replaced) Kromosomin 5 lyhyen haaran deleetio (fi, replaced) Cri-du-chat -oireyhtymä (fi, replaced) Cri-du-chat (fi, replaced) Kattjam-syndromet (sv) Cri-du-chatsyndrom (sv, replaced) Chromosome 5 Short Arm Deletion Syndrome (en, replaced) 5p- Syndrome (en, replaced) Chromosome 5p- Syndrome (en, replaced) Crying Cat Syndrome (en, replaced) Deletion of Short Arm of Chromosome 5 Syndrome (en, replaced) 5p Deletion Syndrome (en, replaced) Syndroma cri-du-chat (la-FI, replaced) X
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