You have selected the view in English
| Descriptor English: | Ellis-Van Creveld Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Ellis-Van Creveld
| ||||||
| Descriptor Portuguese: | Síndrome de Ellis-Van Creveld | ||||||
| Descriptor French: | Syndrome d'Ellis-van Creveld | ||||||
| Entry term(s): |
Chondroectodermal Dysplasia Chondroectodermal Dysplasias Dysplasia, Chondroectodermal Dysplasia, Ellis-Van Creveld Dysplasia, Mesoectodermal Ellis Van Creveld Dysplasia Ellis Van Creveld Syndrome Ellis-Van Creveld Dysplasia Mesoectodermal Dysplasia Mesoectodermal Dysplasias Syndrome, Ellis-Van Creveld |
||||||
| Tree number(s): |
C05.116.099.708.327 C16.131.077.350.398 C16.131.831.350.398 C16.320.850.250.398 C17.800.804.350.398 C17.800.827.250.398 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D004613 | ||||||
| Scope note: | Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed) |
||||||
| Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Public MeSH Note: | 65 |
||||||
| History Note: | 65(63) |
||||||
| DeCS ID: | 22436 | ||||||
| Unique ID: | D004613 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1965/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2016/01/20 |
|
|
Ellis-Van Creveld Syndrome
- Preferred
| Concept UI |
M0007241 |
| Scope note | Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed) |
| Preferred term | Ellis-Van Creveld Syndrome |
| Entry term(s) |
Chondroectodermal Dysplasia Chondroectodermal Dysplasias Dysplasia, Chondroectodermal Dysplasia, Ellis-Van Creveld Dysplasia, Mesoectodermal Ellis Van Creveld Dysplasia Ellis Van Creveld Syndrome Ellis-Van Creveld Dysplasia Mesoectodermal Dysplasia Mesoectodermal Dysplasias Syndrome, Ellis-Van Creveld |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
