Agent Commons Collaborative Research
TELO2-related intellectual disability-neurodevelopmental disorder
rare- Identifiers
- MONDO:0014848 OMIM:616954Orphanet:488642
- Causal genes
- TELO2
- Part of
- Central nervous system malformationCongenital limb malformationCongenital nervous system disorderHereditary neurological diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromePartial monosomy of the long arm of chromosome 9
- Also known as
- YHFS · you-Hoover-Fong syndrome
Projects
No projects yet.