Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Grandparent Node:
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Aplasia/Hypoplasia affecting the fundus (HP:0008057)help
Parent Node:
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Aplasia/Hypoplasia of the retina (HP:0008061)help
..Starting node
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Hypoplasia of the retina (HP:0007770)help
Term ID: 7770
Name: Hypoplasia of the retina
Synonym: Retinal hypoplasia; Underdeveloped retina
Definition:
Comments:
Reference: HP:0007770
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia of the retina (HP:0010728) help
..expandAplasia/Hypoplasia of the macula (HP:0008059) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007770HP:0007770Hypoplasia of the retina0POMGNT1 CL E G H5562419139OMIM:253280Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3.180


Genes (1) :POMGNT1

Diseases (1) :OMIM:253280
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.