Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000084334 Individual ID 00106521 Associated disease ID Diagnosis/Initial - Diagnosis/Definite - Inheritance Isolated (sporadic) Phenotype details Developmental delay/Intellectual disability, Autistic spectrum disorder, Speech/language delay, Microcephaly, Mediofacial hypoplasia, Up-slanting palpebral fissures, hypertelorism, 5th digit clinodactyly; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750) Age/Examination 04y03m (4 years, 3 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Bernt Popp Database submission license No license selected Created by Bernt Popp Date created 2017-07-02 23:04:47 +02:00 (CEST) Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

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