Global Variome shared LOVD

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Phenotype #0000325727 Individual ID 00435540 Associated disease NDD Diagnosis/Initial neurodevelopmental delay Diagnosis/Definite NEDCFSA Phenotype details see paper; ..., bleeding in early pregnancy; birth at term; language/speech delay; motor delay; mild intellectual disability; autism spectrum disorder; attention deficit; hypotonia; joint hypermobility; simian crease, short thumbs, fetal pads, pes planovalgus; no pectus excavatum; hip dysplasia; hypertelorism, microcephaly, small chin, protruding ears; no lip/cleft palate; mild hypermetropic astigmatism; normal hearing; Inheritance Familial Age/Examination 10y (10 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-08-03 13:47:25 +02:00 (CEST) Date last edited N/A

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