Phenotype #0000236308

Individual ID 00311044
Associated disease neuropathy, optic
Phenotype details Caesarian section (HP:0011410); Preeclampsia (HP:0100602); Delayed speech and language development (HP:0000750); Blindness (HP:0000618); Optic nerve hypoplasia (HP:0000609); Strabismus (HP:0000486); Impaired mastication (HP:0005216); Muscular hypotonia (HP:0001252); Autistic behavior (HP:0000729); Attention deficit hyperactivity disorder (HP:0007018); Optic atrophy (HP:0000648)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Age/Examination 21y (21 years)
Age/Diagnosis -
Age/Onset ?
Phenotype/Onset -
Protein -
Owner name Benjamin Billiet
Database submission license No license selected
Created by Benjamin Billiet
Date created 2020-09-14 11:33:51 +02:00 (CEST)
Date last edited 2021-05-05 16:34:12 +02:00 (CEST)

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