Orofaciodigital Syndrome Vii; Ofd7
Facial asymmetry, pseudocleft lip, lobulated tongue, hydronephrosis, delayed development, and low intelligence.
Clinical FeaturesTop most frequent phenotypes and symptoms related to Orofaciodigital Syndrome Vii; Ofd7
- Cleft lip
- Abnormality of the kidney
- Facial asymmetry
- Preauricular skin tag
- Coarse hair
- Polycystic kidney dysplasia
- Abnormality of digit
And another 3 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Orofaciodigital Syndrome Vii; Ofd7 Is also known as ofds vii, whelan syndrome, oral-facial-digital syndrome, type vii.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Sources and references
You can check the following sources for additional information.OMIM ORPHANET MESH Genetic Syndrome Finder
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LONG QT SYNDROME 3; LQT3 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10