| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) | Parent Node:
Craniofacial Abnormalities (D019465) | Parent Node:
Foot Deformities, Congenital (D005532) | Parent Node:
Hand Deformities, Congenital (D006228) | Parent Node:
Intellectual Disability (D008607) | Parent Node:
Joint Instability (D007593) | ..Starting node
.. Van Maldergem Wetzburger Verloes syndrome (C536530)
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Child Nodes:
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Sister Nodes: | ..Achard syndrome (C536012)
| ..Arterial Tortuosity Syndrome (C565942)
| ..Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
| ..Daish Hardman Lamont syndrome (C535770)
| ..Desbuquois syndrome (C535943)
| ..Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism (C563315)
| ..Hemangiomatosis, Cutaneous, with Associated Features (C562438)
| ..Hypospadias-Mental Retardation Syndrome (C563067)
| ..Jaffer Beighton syndrome (C537561)
| ..Megarbane syndrome (C536145)
| ..Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
| ..Panic Disorder with Joint Laxity (C566835)
| ..Patella, Familial Recurrent Dislocation Of (C566816)
| ..Spondyloepimetaphyseal Dysplasia With Joint Laxity (C562968)
| ..Spondyloepiphyseal Dysplasia with Atlantoaxial Instability (C563472)
| ..Van Maldergem Wetzburger Verloes syndrome (C536530)
| ..Young Simpson syndrome (C536717)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 11519 |
| Name: | Van Maldergem Wetzburger Verloes syndrome |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D000015|MESH:D005532|MESH:D006228|MESH:D007593|MESH:D008607|MESH:D019465 |
| TreeNumbers: | C05.330.495/C536530 |C05.390.408/C536530 |C05.550.521/C536530 |C05.660.207/C536530 |C05.660.585.512.380/C536530 |C05.660.585.988.425/C536530 |C10.597.606.643/C536530 |C16.131.077/C536530 |C16.131.621.207/C536530 |C16.131.621.585.380/C536530 |C16.131.621.585.425/C5 |
| Synonyms: | Cerebro-facio-articular syndrome |Cerebrofacioarticular syndrome |Cerebro-facio-articular syndrome of Van Maldergem |Van Maldergem syndrome |
| Slim Mappings: | Congenital abnormality|Mental disorder|Musculoskeletal disease|Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: C536530
MeSH: C536530
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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