Global Variome shared LOVD

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Phenotype #0000143363 Individual ID 00181109 Associated disease MCPH Phenotype details Meckel-syndrome 12 Renal agenesis (HP:0000104), Cerebral hypoplasia (HP:0006872), Cerebellar hypoplasia (HP:0001321), Occipital lobe agenesis, Ureteral agenesis (HP:0012300), Hypoplasia of the uterus (HP:0000013) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Isabel Filges Database submission license No license selected Created by Isabel Filges Date created 2018-10-01 17:46:03 +02:00 (CEST) Date last edited 2018-10-09 20:07:08 +02:00 (CEST)

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