Intellectual Developmental Disorder With Neuropsychiatric Features; Iddnpf
Intellectual developmental disorder with neuropsychiatric features is an autosomal recessive disorder characterized by moderate intellectual disability, relatively mild seizures, and neuropsychiatric abnormalities, such as anxiety, obsessive-compulsive behavior, and autistic features. Mild facial dysmorphic features may also be present (summary by Srour et al., 2017).
Genes related to Intellectual Developmental Disorder With Neuropsychiatric Features; Iddnpf
Clinical FeaturesTop most frequent phenotypes and symptoms related to Intellectual Developmental Disorder With Neuropsychiatric Features; Iddnpf
- Intellectual disability
- Global developmental delay
- Generalized hypotonia
- Depressed nasal bridge
- Downslanted palpebral fissures
- Absent speech
- Thin upper lip vermilion
And another 12 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.
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.
Intellectual Developmental Disorder With Neuropsychiatric Features; Iddnpf Recommended genes panels
|Panel Name, Specifity and genes Tested/covered|
By Fulgent Genetics Fulgent Genetics (United States).
You can get up to -7 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.OMIM 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 VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL SPINOCEREBELLAR ATAXIA 28; SCA28 GELEOPHYSIC DYSPLASIA 1; GPHYSD1 NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY; NLSDM TATTON-BROWN-RAHMAN SYNDROME; TBRS APLASIA CUTIS CONGENITA, NONSYNDROMIC; ACC