Issue 7964 (#8390)

* MONDO:0014606- Spelling Error in Definition

Closes #7964

* Update mondo-edit.obo

* Update mondo-edit.obo

---------

Co-authored-by: Sabrina Toro <[email protected]>

src/ontology/mondo-edit.obo

@@ -337380,7 +337380,7 @@ property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/
 [Term]
 id: MONDO:0014606
 name: intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
-def: "Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by craniofacial dysmorphism (microcephaly, hypotonic facies, strabismus, long and flat malar region, posteriorly rotated ears, flat nasal bridge with broad nasal tip, short philtrum, thin vermillion border, open mouth with down-turned corners, high arched palate, pointed chin), global developmental delay, intellectual disability and variable neurobehavioral abnormalities (autism spectrum disorder, aggressivness, self injury). Additional features include vision abnormalities and variable sensorineural hearing loss, as well as short stature, hypotonia and gastrointestinal manifestations (e.g. poor feeding, gastroesophageal reflux, constipation)." [Orphanet:468678]
+def: "Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by craniofacial dysmorphism (microcephaly, hypotonic facies, strabismus, long and flat malar region, posteriorly rotated ears, flat nasal bridge with broad nasal tip, short philtrum, thin vermillion border, open mouth with down-turned corners, high arched palate, pointed chin), global developmental delay, intellectual disability and variable neurobehavioral abnormalities (autism spectrum disorder, aggressiveness, self injury). Additional features include vision abnormalities and variable sensorineural hearing loss, as well as short stature, hypotonia and gastrointestinal manifestations (e.g. poor feeding, gastroesophageal reflux, constipation)." [Orphanet:468678]
 subset: clingen {source="MONDO:CLINGEN"}
 subset: gard_rare {source="GARD:13774", source="MONDO:GARD"}
 subset: nord_rare {source="MONDO:NORD"}
@@ -337413,6 +337413,7 @@ relationship: excluded_subClassOf MONDO:0015802 {source="DOID:0070067", source="
 relationship: has_characteristic HP:0000006 ! Autosomal dominant inheritance
 relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/hgnc/18801 {source="MONDO:mim2gene_medgen"} ! POGZ
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/5588" xsd:anyURI
+property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7964" xsd:anyURI
 
 [Term]
 id: MONDO:0014607