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Metadata
ID DOID:0060390
Name distal 10q deletion syndrome
Definition A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10.
https://rarediseases.info.nih.gov/diseases/3711/chromosome-10q-deletion
Xrefs

ICD10CM:Q93.5

MESH:C567182

OMIM:609625

ORDO:96148

Subsets

DO_rare_slim

Synonyms

chromosome 10q26 deletion syndrome [EXACT]

distal monosomy 10q [EXACT]

monosomy 10qter [EXACT]

telomeric deletion 10q [EXACT]

terminal chromosome 10q26 deletion syndrome [EXACT]

Parent Relationships

is_a chromosomal deletion syndrome

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