Orofaciodigital Syndrome Vii; Ofd7

Description

Facial asymmetry, pseudocleft lip, lobulated tongue, hydronephrosis, delayed development, and low intelligence.

Clinical Features

Top most frequent phenotypes and symptoms related to Orofaciodigital Syndrome Vii; Ofd7

  • Hypertelorism
  • Clinodactyly
  • Hydronephrosis
  • 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.

Click here to know more about Mendelian.

Incidence and onset information

Not enough data available about incidence and published cases.
No data available about the known clinical features onset.

Alternative names

Orofaciodigital Syndrome Vii; Ofd7 Is also known as ofds vii, whelan syndrome, oral-facial-digital syndrome, type vii.

Researches and researchers

Currently, 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.


Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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 NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1 MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more