Visual loss

Basic details

Preferred term: Visual loss
Alt. terms: loss of vision | visual loss

HPO term: Visual loss
HPO code: HP:0000572

GenIA ID: 696
Last updated on: 2021-12-10 17:55:48

Cross ref. with other ontologies

NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -

Description

Loss of visual acuity (implying that vision was better at a certain timepoint in life). Otherwise the term reduced visual acuity should be used (or a subclass of that).

Hierarchical classification

PARENT terms
TERM

Visual loss

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101376 F 212162 13 Iranian Visual loss Immunodeficiency, common variable, 8 PMID:29461210 [Fam.1:II.2(P2)]; PMID:29528757 [Case 4]; PMID:26707784 [Fam.F:IV.2(P31)]; PMID:26993986 [Fam.F7:II.2(2)]; PMID:28512785 [P9]
103129 F 215101tree icon - Saudi Visual impairment Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.6]
103130 M 215101tree icon - Saudi Visual impairment Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.7]
103131 M 215101tree icon - Saudi Visual impairment Seizures, cortical blindness, microcephaly syndrome PMID:24781755 [Fam.P1:IV.8]
103132 M 215102tree icon - Emirati Visual impairment Seizures, cortical blindness, microcephaly syndrome PMID:26463574 [Fam.MC36500:IV.6(IV.3)]
103776 F 215237tree icon - German Visual impairment Adenosine deaminase 2 deficiency PMID:24552285 [Fam.F:II.1(F-II-1)]
103880 F 215269tree icon 12 Finnish Visual loss Infantile-Onset Multisystem Autoimmune Disease 1 PMID:25038750 [P5]; PMID:25349174 [Fam.1:II.4(Patient 1)]
105013 M 215623tree icon 37 Visual loss Hyper-IgE recurrent infection syndrome 1 PMID:29803798 [Patient(II.2)]
105549 F 215801 12 Caucasian Visual impairment CTLA4 haploinsufficiency with autoimmune infiltration PMID:29200144 [Fam.A:IV.1(P1)]
106847 M 216169tree icon - Caucasian Visual loss Adenosine deaminase 2 deficiency PMID:29963054 [P1(II.1)]

*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).