Search Ontology:
Human Disease
Potocki-Lupski syndrome
- Term ID
- DOID:0060853
- Synonyms
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- 17p11.2 microduplication syndrome
- chromosome 17p11.2 duplication syndrome
- trisomy 17p11.2
- Definition
- A chromosomal duplication syndrome characterized by hypotonia, failure to thrive, mental retardation, pervasive developmental disorders and congenital anomalies that has_material_basis_in contiguous gene syndrome caused by duplication of chromosome 17p11.2. (2)
- References
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- GARD:10145
- MESH:C538355
- MIM:610883
- NCI:C124846
- ORDO:1713
- SNOMEDCT_US_2023_03_01:734016004
- UMLS_CUI:C2931246
- Ontology
- Human Disease ( DOID:0060853 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models