/cranioectodermal dysplasia 1

cranioectodermal dysplasia 1

Rare Disease

MONDO:0021093

Also Known As

Sensenbrenner syndromeCED1IFT122 cranioectodermal dysplasiacranioectodermal dysplasia 1cranioectodermal dysplasia caused by mutation in IFT122cranioectodermal dysplasia type 1Levin syndrome 1

Definition

Any cranioectodermal dysplasia in which the cause of the disease is a mutation in the IFT122 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

IFT122 ↗

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

External Resources

OMIM

OMIM:218330 ↗

Related Diseases

cranioectodermal dysplasia 2

MONDO:0013323

Rare

cranioectodermal dysplasia 3

MONDO:0013573

Rare

cranioectodermal dysplasia 4

MONDO:0013719

Rare

short-rib thoracic dysplasia 16 with or without polydactyly

MONDO:0014915

Rare

cranioectodermal dysplasia 5

MONDO:0976269

Rare

cranioectodermal dysplasia 6

MONDO:0979883

Rare

← Back to All Diseases