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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:syndromic microphthalmia 9
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Accession:DOID:0111807 term browser browse the term
Definition:A syndromic microphthalmia characterized by bilateral clinical anophthalmia, pulmonary hypoplasia or aplasia, cardiac malformations, and diaphragmatic defects that has_material_basis_in homozygous or compound heterozygous mutation in STRA6 on chromosome 15q24.1. (DO)
Synonyms:exact_synonym: Anophthalmia with Pulmonary Hypoplasia;   ISOLATED ANOPHTHALMIA-MICROPHTHALMIA SYNDROME;   MCOPS9;   Matthew-Wood syndrome;   Spear Syndrome;   anophthalmia-pulmonary hypoplasia syndrome;   anophthalmia/microphthalmia and pulmonary hypoplasia;   clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations;   clinical anophthalmia with mild facial dysmorphism and variable malformations of the lung, heart, and diaphragm;   pulmonary agenesis microphthalmi and diaphragmatic defect;   syndromic microphthalmia type 9
 narrow_synonym: MCOPCB8;   PMD MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8;   PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT
 primary_id: MESH:C537768
 alt_id: DOID:0050819;   OMIM:601186
 xref: ORDO:2470
For additional species annotation, visit the Alliance of Genome Resources.



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syndromic microphthalmia 9 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aldh1a3 aldehyde dehydrogenase 1 family, member A3 ISO ClinVar Annotator: match by term: Isolated anophthalmia-microphthalmia syndrome ClinVar PMID:25741868 PMID:28590501 NCBI chr 1:119,982,272...120,017,416
Ensembl chr 1:119,982,277...120,017,436
JBrowse link
G Stra6 signaling receptor and transporter of retinol STRA6 ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Matthew-Wood syndrome | ClinVar Annotator: match by term: Microphthalmia syndromic 9
CTD
OMIM
ClinVar
PMID:11857549 PMID:16199547 PMID:17273977 PMID:17503335 PMID:18316031 More... NCBI chr 8:58,549,743...58,568,861
Ensembl chr 8:58,549,736...58,568,860
JBrowse link
G Wnt7b Wnt family member 7B ISO ClinVar Annotator: match by term: Matthew-Wood syndrome ClinVar PMID:25741868 NCBI chr 7:116,634,817...116,679,089
Ensembl chr 7:116,634,814...116,679,581
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18145
    sensory system disease 6393
      eye disease 2932
        Eye Abnormalities 461
          Anophthalmia 10
            syndromic microphthalmia 9 3
Path 2
Term Annotations click to browse term
  disease 18145
    disease of anatomical entity 17519
      nervous system disease 13182
        sensory system disease 6393
          eye disease 2932
            Eye Abnormalities 461
              microphthalmia 116
                syndromic microphthalmia 64
                  syndromic microphthalmia 9 3
paths to the root