Klippel-Feil Syndrome 3, Autosomal Dominant (KFS3)

Alias:

Kfs3

Klippel-Feil Syndrome, Type 3, Autosomal Dominant

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Klippel-Feil Syndrome 3, Autosomal Dominant, is also known as kfs3. An important gene associated with Klippel-Feil Syndrome 3, Autosomal Dominant is GDF3 (Growth Differentiation Factor 3). Affiliated tissues include bone, and related phenotypes are iris coloboma and chorioretinal coloboma

Related ID：

MALACARDS：KLP006

OMIM：613702

MESH：D007714