Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii

Clinical Features

Top most frequent phenotypes and symptoms related to Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii

  • Intellectual disability
  • Generalized hypotonia
  • Microcephaly
  • Growth delay
  • Micrognathia
  • Strabismus
  • Muscular hypotonia
  • High palate
  • Intrauterine growth retardation
  • Optic atrophy

And another 40 symptoms. If you need more information about this disease we can help you.

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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.

Alternative names

Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii Is also known as osteodysplastic primordial dwarfism, type iii, mopd iii, microcephalic osteodysplastic primordial dwarfism, caroline crachami type, mopd3, mopd, caroline crachami type, microcephalic osteodysplastic primordial dwarfism, sicilian fairy type, mopd, sicilian fairy.

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.


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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TRICHORHINOPHALANGEAL SYNDROME, TYPE I; TRPS1 SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1 CYANOSIS, TRANSIENT NEONATAL; TNCY

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