Phenotype #0000321819

Individual ID 00431213
Associated disease SMS
Phenotype details see paper; ..., obesity, brachydactyly, developmental delay, cognitive impairment, behavioral outbursts, sleep disruption, facial appearance
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite Smith-Magenis syndrome
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-02-03 10:58:30 +01:00 (CET)
Date last edited N/A

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