Global Variome shared LOVD

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Phenotype #0000357112 Individual ID 00472309 Associated disease FTHS Phenotype details see paper; ..., motor retardation; prominent forehead; no brachycephaly; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; no micrognathia; no protruding ears; no kyphosis; no prominent coccyx; no bowing long bones; no short hands; no flexion deformity fingers; club feet; no mitral valve anomaly; no double right outlet; atrial septal defect; auricular pits Diagnosis/Initial Frank-Ter Haar syndrome Inheritance Unknown Diagnosis/Definite − Age/Examination - Age/Diagnosis - 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 2026-01-31 12:03:29 +01:00 (CET) Date last edited N/A

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