| Disease Browser
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Parent Node:
 Foot Deformities, Congenital (D005532) | Parent Node:
Goiter, Nodular (D006044) | Parent Node:
Hand Deformities, Congenital (D006228) | Parent Node:
Polycystic Kidney Diseases (D007690) | ..Starting node
.. Daneman Davy Mancer syndrome (C535986)
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Child Nodes:
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Sister Nodes: | ..Arima syndrome (C537430)
| ..Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome (C565867)
| ..Daneman Davy Mancer syndrome (C535986)
| ..Meckel syndrome type 1 (C536133)
| ..Meckel syndrome type 2 (C536131)
| ..Meckel syndrome type 3 (C536132)
| ..Meckel Syndrome, Type 4 (C567003)
| ..Meckel Syndrome, Type 5 (C566915)
| ..Meckel Syndrome, Type 6 (C567365)
| ..Meckel-Like Cerebrorenodigital Syndrome (C567004)
| ..Polycystic kidney disease, type 1 (C536326)
| ..Polycystic Kidney, Autosomal Dominant (D016891)  3
| ..Polycystic Kidney, Autosomal Recessive (D017044) 3
| ..Polycystic Kidney, Cataract, and Congenital Blindness (C564882)
| ..Potter Type III Polycystic Kidney Disease (C566792)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 2970 |
| Name: | Daneman Davy Mancer syndrome |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D005532|MESH:D006044|MESH:D006228|MESH:D007690 |
| TreeNumbers: | C05.330.495/C535986 |C05.390.408/C535986 |C05.660.585.512.380/C535986 |C05.660.585.988.425/C535986 |C12.777.419.403.875/C535986 |C13.351.968.419.403.875/C535986 |C16.131.621.585.380/C535986 |C16.131.621.585.425/C535986 |C19.874.283.501/C535986 |
| Synonyms: | Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies |Multinodular goiter, cystic renal disease, and digital anomalies |Multinodular Goiter/Cystic Renal Disease/Digital Anomalies |
| Slim Mappings: | Congenital abnormality|Endocrine system disease|Musculoskeletal disease|Urogenital disease (female)|Urogenital disease (male) |
| Reference: |
MedGen: C535986
MeSH: C535986
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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