Global Variome shared LOVD

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Phenotype #0000061488 Individual ID 00081843 Associated disease MCCRP2 Phenotype details Intellectual disability, severe (HP:0010864) Sloping forehead (HP:0000340) Upslanted palpebral fissure (HP:0000582) Blepharophimosis (HP:0000581) Epicanthus (HP:0000286) Prominent nose (HP:0000448) Micrognathia (HP:0000347) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Bayram Toraman Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Bayram Toraman Date created 2016-10-28 14:56:56 +02:00 (CEST) Date last edited 2016-11-08 23:14:49 +01:00 (CET)

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