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DOID:0060589 - Yunis-Varon syndrome
Disease Ontology Definition:A syndrome characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. It is usually lethal in infancy and has_material_basis_in homozygous or compound heterozygous mutation in the FIG4 gene on chromosome 6q21.
Synonyms: cleidocranial dysplasia-micrognathia-absent thumbs syndrome, cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
Xenbase Genes
:
vac14,
fig4
| MONDO:0008995 - Yunis-Varon syndrome |
| MIM:216340 - YUNIS-VARON SYNDROME; YVS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)