loading...| Preferred Name |
Cri-Du-Chat syndrome |
|
| Synonyms |
5p partial monosomy syndrome |
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| Definitions |
OMIM mapping confirmed by DO. [SN]. A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat. |
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| ID |
http://purl.obolibrary.org/obo/DOID_12580 |
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| comment |
OMIM mapping confirmed by DO. [SN]. |
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| database_cross_reference |
SNOMEDCT_US_2020_03_01:70173007 UMLS_CUI:C0010314 OMIM:123450 MESH:D003410 ICD10CM:Q93.4 ICD9CM:758.31 GARD:6213 NCI:C34518 |
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| has exact synonym |
5p partial monosomy syndrome chromosome 5p deletion syndrome 5p deletion syndrome Cri-du-chat syndrome chromosome 5 short arm deletion syndrome |
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| has_obo_namespace |
disease_ontology |
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| id |
DOID:12580 |
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| imported from | ||
| in_subset | ||
| label |
Cri-Du-Chat syndrome |
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| notation |
DOID:12580 |
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| prefLabel |
Cri-Du-Chat syndrome |
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| textual definition |
A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat. |
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| subClassOf |
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