Phenotype #0000036649

Individual ID 00049867
Associated disease RTS2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Age/Examination 02y (2 years)
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details poikiloderma, microdontia, abnormalities of the long bones, short stature, delayed motor development, nutritional problems, osteosarcoma
Protein -
Owner name Sabina Gallati, Prof.
Database submission license No license selected
Created by Sabina Gallati, Prof.
Date created 2015-09-13 16:39:06 +02:00 (CEST)
Date last edited 2016-01-26 02:58:19 +01:00 (CET)

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