Filippi syndrome

Summary
Synonym
  • Scott craniodigital syndrome with mental retardation
  • type 1 syndactyly-microcephaly-intellectual disability syndrome
Definition
A syndrome characterized by short stature, microcephaly, syndactyly, intellectual disability, pre- and postnatal growth failure, and facial dysmorphism that has_material_basis_in homozygous or compound heterozygous mutation in the CKAP2L gene on chromosome 2q14.1.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0112194
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
150468 CKAP2L cytoskeleton associated protein 2 like
Displaying 1 entry
Gene ID Gene Symbol Description Source
70466 Ckap2l cytoskeleton associated protein 2-like

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024