Rosselli-Gulienetti syndrome (Q100044): Difference between revisions
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Síndrome de Rosselli-Gulienetti é um tipo de displasia ectodérmica caracterizada por anidrose, hipotricose, fenda e lábio palatino, microdontia e sindactilia. | |||
| description / en | description / en | ||
Rosselli-Gulienetti syndrome is a type of ectodermal dysplasia characterised by anhidrosis, hypotrichosis, cleft and lip palate, microdontia and syndactyly. | |||
Revision as of 16:43, 16 August 2026
Rosselli-Gulienetti syndrome is a type of ectodermal dysplasia characterised by anhidrosis, hypotrichosis, cleft and lip palate, microdontia and syndactyly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1430451924 |
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| English | Rosselli-Gulienetti syndrome |
Rosselli-Gulienetti syndrome is a type of ectodermal dysplasia characterised by anhidrosis, hypotrichosis, cleft and lip palate, microdontia and syndactyly. |
