Phenotype #0000051301

Individual ID 00065194
Associated disease ID
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details mild autism (HP:0000729), Microcephaly (HP:0000252), Feeding difficulties (HP:0011968), abnormality of vision (HP:0000252), obesity (HP:0001513); severe intellectual disability (HP:0010864); motor delay (HP:0001270); moderate speech delay (HP:0000750)
Age/Examination 02y (2 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Pieter Klap
Database submission license No license selected
Created by Pieter Klap
Date created 2016-05-20 15:48:59 +02:00 (CEST)
Date last edited 2020-05-12 12:33:06 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.