Phenotype #0000308759

Individual ID 00417244
Associated disease ID
Diagnosis/Initial intellectual disability
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details Global developmental delay (HP:0001263); ; no Seizure (-HP:0001250); no Sensorineural hearing impairment (-HP:0000407); Microcephaly (HP:0000252) ; Ophthalmological anomalies (bilateral iris cysts)
Age/Examination 00y14m (14 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Fernanda Soledad Jalil
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Fernanda Soledad Jalil
Date created 2022-09-14 15:36:48 +02:00 (CEST)
Date last edited 2022-11-11 12:45:59 +01:00 (CET)

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