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BioAssay Ontology
Last uploaded:
February 21, 2024
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Preferred Name | Cri-Du-Chat syndrome | |
Synonyms |
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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Definitions |
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. OMIM mapping confirmed by DO. [SN]. |
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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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