Search Ontology:
Human Disease
Mulchandani-Bhoj-Conlin syndrome
- Term ID
- DOID:0111714
- Synonyms
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- maternal uniparental disomy of chromosome 20
- maternal UPD(20)
- MBCS
- UPD(20)mat
- Definition
- A syndrome characterized by prenatal growth restriction, severe short stature with proportional head circumference, and profound feeding difficulty that has_material_basis_in heterozygous mutation in an imprinting region on chromosome 20q11-q13. https://www.ncbi.nlm.nih.gov/pubmed/26248010
- References
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- MIM:617352
- ORDO:96186
- SNOMEDCT_US_2023_03_01:715735007
- UMLS_CUI:C4275029
- Ontology
- Human Disease ( DOID:0111714 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models