Global Variome shared LOVD

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Phenotype #0000016191 Individual ID 00017840 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details intellectual disability syndrome of congenital microcephaly, low anterior hairline, bitemporal narrowing, low-set protruding ears, strabismus and tented thick eyebrows with sparse hair in their medial segment. Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Ohad S Birk Database submission license No license selected Created by Ohad S Birk Date created 2014-07-03 04:48:37 +02:00 (CEST) Date last edited 2019-03-29 21:08:30 +01:00 (CET)

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