Global Variome shared LOVD
APOA2 (apolipoprotein A-II)
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Curator:
Dorota Rowczenio
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Phenotype #0000288565
Individual ID
00395365
Associated disease
FOP
Phenotype details
see paper; ..., typical great toe malformation, short thumbs/cervical spine fusions, broad femoral necks/knee osteochondroma; 1y6m-ectopic ossification neck, 7 lesions; no deafness; persistence primary teeth, hypertrichosis
Diagnosis/Initial
classic fibrodysplasia ossificans progressiva
Inheritance
Unknown
Diagnosis/Definite
FOP
Age/Examination
13y (13 years)
Age/Diagnosis
6m
Age/Onset
-
Phenotype/Onset
-
Protein
-
Owner name
Johan den Dunnen
Database submission
license
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International
Created by
Johan den Dunnen
Date created
2021-12-05 12:53:42 +01:00 (CET)
Date last edited
N/A
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