/neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity

neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity

MONDO:0030046

Also Known As

NEDBASSNEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITYneurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

PTPN23 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:618890 ↗

Related Diseases

microcephaly and chorioretinopathy

MONDO:0000181

Rare

microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

MONDO:0007918

Rare

autosomal dominant primary microcephaly

MONDO:0007988

Rare

Prader-Willi syndrome

MONDO:0008300

Rare

Smith-Magenis syndrome

MONDO:0008434

Rare

microcephalic osteodysplastic primordial dwarfism type I

MONDO:0008871

Rare

← Back to All Diseases