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The way concept relations are shown:
The way concept relations are shown:
Ellis-Van Creveld Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome 21 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome ∟ ∟ ∟ ∟ ∟ Ellis-Van Creveld Syndrome |
Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
historyNote*: | 65(63)
X |
publicMeSHNote*: | 65
X |
Scope note: | Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed)
X |
activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateEstablished*: | 1965-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Kondroektodermaalinen dysplasia (fi) XChondroectodermal Dysplasia (en, replaced) Síndrome de Ellis-Van Creveld (es) σύνδρομο Ellis-Van Creveld (el) Ellis-Van-Creveld-Syndrom (de) Ellisův-van Creveldův syndrom (cs) Displasia Condroectodérmica (es, replaced) Dysplasie, chondroektodermale (de, replaced) Chondroektodermale Dysplasie (de, replaced) |
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