| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) | Parent Node:
Growth Disorders (D006130) | Parent Node:
Intellectual Disability (D008607) | Parent Node:
Microcephaly (D008831) | Parent Node:
Scoliosis (D012600) | Parent Node:
Synostosis (D013580) | ..Starting node
.. Tsukahara Syndrome (C566376)
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Child Nodes:
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Sister Nodes: | ..Antley-Bixler Syndrome Phenotype (D054882)  2
| ..Banki Syndrome (C566228)
| ..Coronal synostosis, syndactyly and jejunal atresia (C536445)
| ..Craniosynostoses (D003398) 64
| ..Der Kaloustian Mcintosh Silver syndrome (C538217)
| ..Humeroradial Multiple Synostosis Syndrome (C565509)
| ..Humeroradial Synostosis with Craniofacial Anomalies (C566888)
| ..Jorgenson Lenz syndrome (C536292)
| ..Mesomelia-synostoses syndrome (C537348)
| ..MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
| ..Multiple synostoses syndrome 2 (C537380)
| ..Multiple Synostoses Syndrome 3 (C567839)
| ..NOG-Related-Symphalangism Spectrum Disorder (C536943)
| ..Patella aplasia, coxa vara, tarsal synostosis (C536307)
| ..Prata Libéral Gonçalves syndrome (C538277)
| ..Radioulnar Synostosis (C562408)
| ..Radioulnar synostosis retinal pigment abnormalities (C536270)
| ..Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia (C565328)
| ..Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male (C564557)
| ..Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia (C564856)
| ..Ramer Ladda syndrome (C535284)
| ..Spondylocarpotarsal synostosis (C535780)
| ..Symphalangism of Toes (C566101)
| ..Symphalangism with Multiple Anomalies of Hands and Feet (C566098)
| ..Syndactyly (D013576) 69
| ..Synostoses, tarsal, carpal, and digital (C538156)
| ..Synostosis of Talus and Calcaneus with Short Stature (C566089)
| ..Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly (C566090)
| ..Tsukahara Syndrome (C566376)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 11301 |
| Name: | Tsukahara Syndrome |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D000015|MESH:D006130|MESH:D008607|MESH:D008831|MESH:D012600|MESH:D013580 |
| TreeNumbers: | C05.116.099.370.894/C566376 |C05.116.900.800.875/C566376 |C05.660.207.620/C566376 |C05.660.906/C566376 |C10.500.507.400.500/C566376 |C10.597.606.643/C566376 |C16.131.077/C566376 |C16.131.621.207.620/C566376 |C16.131.621.906/C566376 |C16.131.666.507.400.500/C56637 |
| Synonyms: | Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation |
| Slim Mappings: | Congenital abnormality|Mental disorder|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms |
| Reference: |
MedGen: C566376
MeSH: C566376
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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