Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) | Parent Node: Facial Asymmetry (D005146) | Parent Node: Language Development Disorders (D007805) | Parent Node: Strabismus (D013285) | ..Starting node ..Mehes syndrome (C536146)
| Child Nodes:
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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: | 6903 |
Name: | Mehes syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D005146|MESH:D007805|MESH:D013285 |
TreeNumbers: | C10.292.562.887/C536146 |C10.597.606.150.500.550/C536146 |C11.590.810/C536146 |C16.131.077/C536146 |C23.300.505/C536146 |C23.888.592.604.150.500.550/C536146 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Eye disease|Nervous system disease|Pathology (anatomical condition)|Signs and symptoms |
Reference: |
MedGen: C536146
MeSH: C536146
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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