Search Ontology:
Human Disease
syndromic X-linked intellectual disorder Lujan-Fryns-type
- Term ID
- DOID:0080985
- Synonyms
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- Definition
- A syndromic X-linked intellectual disability that is characterized by a tall, marfanoid stature, distinct facial dysmorphism and behavioral problems and that has_material_basis_in hemizygous mutation in the MED12 gene on chromosome Xq13. Opitz-Kaveggia syndrome is an allelic disorder with an overlapping phenotype. (2)
- References
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- GARD:3307
- MIM:309520
- ORDO:776
- Ontology
- Human Disease ( DOID:0080985 )
- is a type of
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Genes Involved
Zebrafish Models