MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
expandcone-rod dystrophy (MONDO:0015993)
Parent Node:
expandX-linked disease (MONDO:0000425)
..Starting node
..expandX-linked cone-rod dystrophy ()

       Child Nodes:
........expandblue cone monochromacy ()
........expandX-linked cone-rod dystrophy 1 ()
........expandX-linked cone-rod dystrophy 2 ()
........expandX-linked cone-rod dystrophy 3 ()



 Sister Nodes: 
..expandAarskog-Scott syndrome, X-linked ()
..expandchoroideremia ()
..expandcone dystrophy, X-linked, with tapetal-like sheen ()
..expanddiabetes insipidus, nephrogenic, X-linked ()
..expanddyskeratosis congenita, X-linked ()
..expandepidermodysplasia verruciformis, X-linked ()
..expandexudative vitreoretinopathy 2, X-linked ()
..expandhemophilia A ()
..expandmacular dystrophy, X-linked ()
..expandnon-syndromic X-linked intellectual disability ()
..expandOgden syndrome ()
..expandWiskott-Aldrich syndrome ()
..expandX-linked acrogigantism due to Xq26 microduplication ()
..expandX-linked adrenoleukodystrophy ()
..expandX-linked Alport syndrome ()
..expandX-linked central congenital hypothyroidism with late-onset testicular enlargement ()
..expandX-linked cerebellar ataxia ()
..expandX-linked chondrodysplasia punctata ()
..expandX-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome ()
..expandX-linked cone-rod dystrophy ()
..expandX-linked congenital hemolytic anemia ()
..expandX-linked congenital stationary night blindness ()
..expandX-linked distal hereditary motor neuropathy ()
..expandX-linked dominant disease ()
..expandX-linked Ehlers-Danlos syndrome ()
..expandX-linked Emery-Dreifuss muscular dystrophy ()
..expandX-linked erythropoietic protoporphyria ()
..expandX-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome ()
..expandX-linked hyper-IgM syndrome ()
..expandX-linked hypohidrotic ectodermal dysplasia ()
..expandX-linked hypophosphatemic rickets (recessive or dominant) ()
..expandX-linked ichthyosis syndrome ()
..expandX-linked lethal multiple pterygium syndrome ()
..expandX-linked lymphoproliferative syndrome ()
..expandX-linked nonsyndromic deafness ()
..expandX-linked Opitz G/BBB syndrome ()
..expandX-linked recessive disease ()
..expandX-linked retinoschisis ()
..expandX-linked severe congenital neutropenia ()
..expandX-linked sideroblastic anemia ()
..expandX-linked spondyloepimetaphyseal dysplasia ()
..expandX-linked syndromic intellectual disability ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:21155
Name:X-linked cone-rod dystrophy
Definition:X-linked form of cone-rod dystrophy.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:cone-rod dystrophy, X-linked
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal