Cleft Lip/palate-Ectodermal Dysplasia Syndrome (CLPED1)

Alias:

Orofacial Cleft 7

Zlotogora-Ogur Syndrome

Clped1

Syndactyly-Ectodermal Dysplasia-Cleft/lip Palate

Cleft Lip/palate-Syndactyly-Pili Torti Syndrome

Cleft Lip-Palate-Ectodermal Dysplasia Syndrome

Ectodermal Dysplasia, Margarita Island Type

Ectodermal Dysplasia Margarita Type

Ectodermal Dysplasia 4

Ed4

Ectodermal Dysplasia, Cleft Lip and Palate, Mental Retardation, and Syndactyly

Non-Syndromic Cleft Lip with or Without Cleft Palate 7

Syndactyly-Ectodermal Dysplasia-Cleft Lip/palate

Ectodermal Dysplasia 4, Hair/nail Type

Margarita Type of Ectodermal Dysplasia

Zlotogora-Zilberman-Tenenbaum Syndrome

Margarita Island Ectodermal Dysplasia

Non-Syndromic Cleft Lip/palate 7

Non-Syndromic Orofacial Cleft 7

Ectodermal Dysplasia, Type 4

Ectodermal Dysplasia Type 4

Ectd4

Edmi

Ofc7

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cleft Lip/palate-Ectodermal Dysplasia Syndrome, also known as orofacial cleft 7, is related to cleft lip/palate and ectodermal dysplasia. An important gene associated with Cleft Lip/palate-Ectodermal Dysplasia Syndrome is NECTIN1 (Nectin Cell Adhesion Molecule 1), and among its related pathways/superpathways are PAK Pathway and Sertoli-Sertoli Cell Junction Dynamics. Affiliated tissues include skin and bone, and related phenotypes are macrotia and cleft upper lip

Related ID：

MALACARDS：CLF037

OMIM：225060

MESH：C563464