corneal opacification and other ocular anomalies

sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis

corneal opacification and other ocular anomalies is …
instance of (P31):
class of diseaseQ112193867

sublass of (P279):
genetic diseaseQ200779
monogenic diseaseQ1225194
eye diseaseQ3041498
sclerocorneaQ7434154

External links are
P699Disease Ontology IDDOID:0060648
P2888exact matchhttp://identifiers.org/doid/DOID:0060648
http://purl.obolibrary.org/obo/DOID_0060648
P2671Google Knowledge Graph ID/g/122z_qh0
P494ICD-10H17.9
P5270Mondo IDMONDO_0000817
P492OMIM ID107250
107250

P1995health specialtyophthalmologyQ161437
P5008on focus list of Wikimedia projectWikiProject MedicineQ4099686

Reverse relations

subclass of (P279)
Q102293893anterior segment dysgenesis 1
Q102293240anterior segment dysgenesis 2
Q102293506anterior segment dysgenesis 3
Q102296274anterior segment dysgenesis 4
Q102294020anterior segment dysgenesis 5
Q55785185anterior segment dysgenesis 6
Q55998736anterior segment dysgenesis 7
Q55785186anterior segment dysgenesis 8

Q21173555phenacyl chloride exposurehas effectP1542
Q21173555phenacyl chloride exposuresymptoms and signsP780

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