OBO ID: DOID:0060417 |
Term Name: | 3p deletion syndrome | Search Ontology: | |
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Definition: | A chromosomal deletion syndrome that has_material_basis_in a contiguous gene deletion syndrome involving chromosome 3pter-p25 and is characterized by low birth weight, microcephaly, trigonocephaly, hypotonia, psychomotor and growth retardation, ptosis, telecanthus, downslanting palpebral fissures, and micrognathia. (2) | ||
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Ontology: | Human Disease ( DOID:0060417 ) |
OTHER 3p deletion syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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