Phenotype #0000029097

Individual ID 00038702
Associated disease ICF4
Phenotype details facial anomalies (HP:0001999), no gastrointestinal problems, infections (otitis, pneumonia); IgG 0.91 g/l, IgA <0.04 g/l, IgM 0.04 g/l; cytogenetic abnormalities include translocations, deletions
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Birth/Weight 3830g
Infections no
Protein -
Development no
Intellectual_dis yes
Owner name Peter Thijssen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-05-22 11:11:53 +02:00 (CEST)
Date last edited 2015-07-05 12:05:37 +02:00 (CEST)

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