Phenotype #0000321035

Individual ID 00430227
Associated disease KS
Diagnosis/Initial Kallmann syndrome
Diagnosis/Definite Kallmann syndrome
Phenotype details Micropenis; anosmia; low nose bridge; hearing loss; mild cubitus valgus; metacarpal sign; testicular hypotrophy
Inheritance Familial, autosomal dominant
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Dongye He
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Dongye He
Date created 2023-01-16 04:29:21 +01:00 (CET)
Date last edited 2023-01-17 12:15:33 +01:00 (CET)

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