MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 8
OrphanetNr:
OMIM Id: 616281
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0000252) Microcephaly 832 / 7739
2
 (HPO:0002069) Generalized tonic-clonic seizures 96 / 7739
3
 (HPO:0001249) Intellectual disability 1089 / 7739
4
 (HPO:0001298) Encephalopathy 72 / 7739
5
 (HPO:0001263) Global developmental delay 853 / 7739
6
 (HPO:0001344) Absent speech 57 / 7739
7
 (HPO:0001508) Failure to thrive 454 / 7739
8
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: