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CRADD

CASP2 and RIPK1 domain containing adaptor with death domain

HCNC Approved Symbol
CRADD (HGNC:2340)
Genomic Coordinates
12:93,677,375 - 93,894,840 (12q22)
Synonyms
RAIDD
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly
614499AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the CRADD gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results