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MedGen

National Center for Biotechnology Information

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Items: 3

Select item 3378881.

Fundus dystrophy, pseudoinflammatory, recessive form

MedGen UID:: 337888
•Concept ID:: C1849694
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 3230312.

Peripheral cone dystrophy

MedGen UID:: 323031
•Concept ID:: C1836946
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 2329383.

Peripheral retinal degeneration

Degeneration of the peripheral retina. [from NCI]

MedGen UID:: 232938
•Concept ID:: C1320640
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

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"Peripheral retinal degeneration"[Clinical Features] OR 232938[ui... (3)
"Peripheral retinal degeneration"[Clinical Features] OR 232938[uid]
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MedGen
Concise Conserved Domain Links for Protein (Select 489321005) (1)
Conserved Domains
Protein Family Models for Protein (Select 489321005) (8)
Protein Family Models

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