Phenotype #0000242201

Individual ID 00320155
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Global developmental delay (HP:0001263); Delayed speech and language development (HP:0000750); Muscular hypotonia (HP:0001252); Difficulty walking (HP:0002355); Microcephaly (HP:0000252); Strabismus (HP:0000486); Hypotelorism (HP:0000601); Long philtrum (HP:0000343); Thin upper lip vermilion (HP:0000219); Encopresis (HP:0040183); Long eyelashes (HP:0000527)
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name IMGAG
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by IMGAG
Date created 2020-11-23 17:38:17 +01:00 (CET)
Date last edited 2020-12-08 10:25:34 +01:00 (CET)

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