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Human Disease

developmental delay, hypotrophy, and dysmorphic features without Moebius syndrome

Term ID
DOID:0081264
Synonyms
Definition
A syndrome that is characterized by developmental delay, hypotrophy, and dysmorphic features and that has_material_basis_in homozygous ultra-rare REV3L variant (T2753R). https://pubmed.ncbi.nlm.nih.gov/33474647/
References
Ontology
Human Disease   ( DOID:0081264 )
Relationships
is a type of
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Genes Involved
Zebrafish Models