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 | 215101![]() |
- | Saudi | Visual impairment | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.6] |
103130 | M | 215101![]() |
- | Saudi | Visual impairment | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.7] |
103131 | M | 215101![]() |
- | Saudi | Visual impairment | Seizures, cortical blindness, microcephaly syndrome | PMID:24781755 [Fam.P1:IV.8] |
103132 | M | 215102![]() |
- | Emirati | Visual impairment | Seizures, cortical blindness, microcephaly syndrome | PMID:26463574 [Fam.MC36500:IV.6(IV.3)] |
103776 | F | 215237![]() |
- | German | Visual impairment | Adenosine deaminase 2 deficiency | PMID:24552285 [Fam.F:II.1(F-II-1)] |
103880 | F | 215269![]() |
12 | Finnish | Visual loss | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:25038750 [P5]; PMID:25349174 [Fam.1:II.4(Patient 1)] |
105013 | M | 215623![]() |
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 | 216169![]() |
- | 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).