Carney Complex Variant (CACOV)

Carney Complex Variant(来自ICD-11)
别称:
Carney Complex
Carney Syndrome
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
Carney Complex, Type 1
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
Carney Complex, Type 2
Name Syndrome
Lamb Syndrome
Cacov
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
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References Literature
Carney Complex Variant, also known as carney complex, is related to pigmented nodular adrenocortical disease, primary, 1 and pituitary gigantism. An important gene associated with Carney Complex Variant is MYH8 (Myosin Heavy Chain 8), and among its related pathways/superpathways are Metabolism and ERK Signaling. Affiliated tissues include skin and pituitary, and related phenotypes are pigmented micronodular adrenocortical disease and multiple cafe-au-lait spots
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MALACARDS
AD
Newborn
<1/1000000
50
610
17

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