Global Variome shared LOVD
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
View all genes
Create a new gene entry
View all transcripts
Create a new transcript information entry
View all variants
View all variants affecting transcripts
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
Create a new disease information entry
View available phenotype columns
View all screenings
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Phenotype #0000285379
Individual ID
00392101
Associated disease
XLHR
Phenotype details
see paper; ..., severe bone phenotype, height (SD-3.84), tubular reabsorption of phosphate 0.66, 25 hydroxy vitamin D 37.5 ng/mL, parathyroid hormone 42 pg/mL, alkaline phosphatase 534, nephrocalcinosis after treatment, no hyperparathyroidism
Diagnosis/Initial
hypophosphatemic rickets
Inheritance
Isolated (sporadic)
Diagnosis/Definite
XLHR
Age/Examination
-
Age/Diagnosis
14y
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
2021-11-21 10:41:24 +01:00 (CET)
Date last edited
N/A
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators