Global Variome shared LOVD

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Phenotype #0000290715 Individual ID 00397591 Associated disease NFTC Phenotype details Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Normophosphatemic familial tumoral calcinosis Age/Examination 06y (6 years) Age/Diagnosis 06y Age/Onset 06y Phenotype/Onset Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 Protein - Owner name Litika Vermani Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Litika Vermani Date created 2021-12-26 21:18:10 +01:00 (CET) Date last edited 2021-12-28 16:26:14 +01:00 (CET)

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