Phenotype #0000289369

Individual ID 00396203
Associated disease LPRD1
Phenotype details Microcephaly, Pulmonic stenosis, Ventricular septal defect, Cryptorchidism, Anal stenosis, Delayed speech and language development
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 01y (1 year)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2021-12-15 11:37:12 +01:00 (CET)
Date last edited 2021-12-15 16:53:44 +01:00 (CET)

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