Global Variome shared LOVD

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Phenotype #0000346557 Individual ID 00458112 Associated disease KAL Phenotype details Hypogonadism, Anosmia, Hypopigmented skin patches, Premature graying of hair, Sensorineural hearing impairment, Hyposmia, Primary amenorrhea Diagnosis/Initial Kallmann syndrome Inheritance Familial, autosomal dominant Diagnosis/Definite WS4C Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Ludovico Graziani Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Ludovico Graziani Date created 2024-12-02 14:18:57 +01:00 (CET) Date last edited 2024-12-03 10:05:56 +01:00 (CET)

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