Disease Browser
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Parent Node: Acro-Osteolysis (D030981) | Parent Node: Blepharoptosis (D001763) | Parent Node: Craniofacial Abnormalities (D019465) | Parent Node: Decalcification, Pathologic (D003649) | Parent Node: Intellectual Disability (D008607) | Parent Node: Strabismus (D013285) | ..Starting node ..Van Bogaert-Hozay syndrome (C536526)
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Sister Nodes: | ..Carnevale syndrome (C535586)
| ..Esotropia (D004948) 1
| ..Exotropia (D005099)
| ..Hemifacial Hyperplasia With Strabismus (C564199)
| ..Krauss Herman Holmes syndrome (C537618)
| ..McPherson Robertson Cammarano syndrome (C538161)
| ..Mehes syndrome (C536146)
| ..MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
| ..Ptosis, Strabismus, And Ectopic Pupils (C566736)
| ..Singh Chhaparwal Dhanda syndrome (C537341)
| ..Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease (C566677)
| ..Van Bogaert-Hozay syndrome (C536526)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11511 |
Name: | Van Bogaert-Hozay syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D001763|MESH:D003649|MESH:D008607|MESH:D013285|MESH:D019465|MESH:D030981 |
TreeNumbers: | C05.116.099.052/C536526 |C05.116.198.247.400/C536526 |C05.116.264.579.052/C536526 |C05.660.207/C536526 |C10.292.562.887/C536526 |C10.597.606.643/C536526 |C11.338.204/C536526 |C11.590.810/C536526 |C16.131.621.207/C536526 |C18.452.174.289/C536526 |C23.888.592.604.64 |
Synonyms: | Acro-osteolysis-facial dysplasia syndrome |Hozay's syndrome |
Slim Mappings: | Congenital abnormality|Eye disease|Mental disorder|Metabolic disease|Musculoskeletal disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C536526
MeSH: C536526
OMIM: 277150;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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