MCID: PX6001

Pax6-Related Anophthalmia malady

Genetic diseases, Rare diseases, Fetal diseases categories

Aliases & Classifications for Pax6-Related Anophthalmia

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Pax6-Related Anophthalmia, Aliases & Descriptions:

Name: Pax6-Related Anophthalmia 20


Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic diseases, Rare diseases, Fetal diseases


Summaries for Pax6-Related Anophthalmia

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MalaCards based summary: Pax6-Related Anophthalmia An important gene associated with Pax6-Related Anophthalmia is PAX6 (paired box 6).

Related Diseases for Pax6-Related Anophthalmia

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Diseases in the Anophthalmia Plus Syndrome family:

pax6-related anophthalmia

Symptoms for Pax6-Related Anophthalmia

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Drugs & Therapeutics for Pax6-Related Anophthalmia

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Drug clinical trials:

Search ClinicalTrials for Pax6-Related Anophthalmia

Search NIH Clinical Center for Pax6-Related Anophthalmia

Genetic Tests for Pax6-Related Anophthalmia

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Genetic tests related to Pax6-Related Anophthalmia:

id Genetic test Affiliating Genes
1 Pax6-Related Anophthalmia20 PAX6

Anatomical Context for Pax6-Related Anophthalmia

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Animal Models for Pax6-Related Anophthalmia or affiliated genes

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Publications for Pax6-Related Anophthalmia

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Variations for Pax6-Related Anophthalmia

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Expression for genes affiliated with Pax6-Related Anophthalmia

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Search GEO for disease gene expression data for Pax6-Related Anophthalmia.

Pathways for genes affiliated with Pax6-Related Anophthalmia

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Compounds for genes affiliated with Pax6-Related Anophthalmia

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GO Terms for genes affiliated with Pax6-Related Anophthalmia

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Products for genes affiliated with Pax6-Related Anophthalmia

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies
  • Proteins
  • Kits and Assays

Sources for Pax6-Related Anophthalmia

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3CDC
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCIt
39NDF-RT
42NINDS
43Novoseek
45OMIM
46OMIM via Orphanet
50PubMed
51QIAGEN
56SNOMED-CT via Orphanet
60UMLS
61UMLS via Orphanet