Phenotype #0000051358

Individual ID 00065251
Associated disease CDG2
Phenotype details Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), mild dysmorphic features (HP:0001999), liver failure (HP:0001399)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-05-24 12:04:13 +02:00 (CEST)
Date last edited 2017-03-19 17:43:57 +01:00 (CET)

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