Remove subclass of Fanconi Anemia

Closes #7639

- excluded_SubclassOf Telomere Syndrome
- Added PMID:29804726 and ORCID

- excluded_SubclassOf dysostosis
- Added ORCID

src/ontology/mondo-edit.obo

@@ -436943,12 +436943,12 @@ is_a: MONDO:0001713 {source="DOID:13636", source="MESH:D005199", source="Orphane
 is_a: MONDO:0003225 {source="PMID:31953710"} ! bone marrow disorder
 is_a: MONDO:0005570 ! hematologic disorder
 is_a: MONDO:0015161 {source="Orphanet:84"} ! multiple congenital anomalies/dysmorphic syndrome without intellectual disability
-is_a: MONDO:0018234 ! dysostosis
 is_a: MONDO:0019054 ! congenital limb malformation
 is_a: MONDO:0021190 {source="MESH:D005199", source="MONDO:Redundant", source="NCIT:C62505"} ! DNA repair disease
-is_a: MONDO:0100137 {source="PMID:29804726"} ! telomere syndrome
 relationship: disease_has_basis_in_disruption_of GO:0006281 {source="https://orcid.org/0000-0002-6601-2165"} ! DNA repair
+relationship: excluded_subClassOf MONDO:0018234 {source="https://orcid.org/0000-0002-0587-4693"} ! dysostosis
 relationship: excluded_subClassOf MONDO:0019289 {source="Orphanet:84", source="https://orcid.org/0000-0001-5208-3432"} ! hyperpigmentation of the skin
+relationship: excluded_subClassOf MONDO:0100137 {source="PMID:29804726", source="https://orcid.org/0000-0002-0587-4693"} ! telomere syndrome
 relationship: has_characteristic MONDO:0021136 ! rare
 relationship: has_characteristic MONDO:0021152 {source="OMIMPS:227650"} ! inherited
 property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/5682" xsd:anyURI