Disease #05050 (CFEOM3A (fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A)), OMIM:600638)

Official abbreviation CFEOM3A
Name fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A)
OMIM ID 600638
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TUBB3
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00100445 - - - F ? - - - - - - CFEOM3A Aplasia/Hypoplasia of the corpus callosum;Abnormality of olfactory lobe morphology; Abnormality of the seventh cranial nerve; abnormality of the cranial nerve;neurodevelopmental delay;facial diplegia;intellectual disability, moderate;ptosis;strabismus;nistagmus;dysmorphic facies TUBB3 TUBB3 1 1 Enza Maria Valente
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