MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandgenetic macular dystrophy (MONDO:0020242)
..Starting node
..expandunclassified primitive or secondary maculopathy ()

       Child Nodes:
........expandautosomal dominant osteopetrosis 2 ()
........expandBardet-Biedl syndrome ()
........expandcone-rod dystrophy ()
........expandcongenital hypotrichosis with juvenile macular dystrophy ()
........expandcystoid macular edema ()
........expandenhanced S-cone syndrome ()
........expandFarber lipogranulomatosis ()
........expandfoveal hypoplasia-presenile cataract syndrome ()
........expandgalactosialidosis ()
........expandGM1 gangliosidosis ()
........expandHermansky-Pudlak syndrome 2 ()
........expandinfantile Refsum disease ()
........expandKrabbe disease ()
........expandLaurence-Moon syndrome ()
........expandLeigh disease ()
........expandmetachromatic leukodystrophy ()
........expandmucolipidosis type IV ()
........expandneuronal ceroid lipofuscinosis ()
........expandNiemann-Pick disease type C ()
........expandRubinstein-Taybi syndrome ()
........expandSjogren-Larsson syndrome ()
........expandSorsby's fundus dystrophy ()
........expandX-linked retinoschisis ()
........expandZellweger syndrome ()



 Sister Nodes: 
..expandAICA-ribosiduria ()
..expandbenign concentric annular macular dystrophy ()
..expandcolobomatous and areolar dystrophy ()
..expandcone dystrophy ()
..expandEEM syndrome ()
..expandfamilial flecked retinopathy ()
..expandmacular corneal dystrophy ()
..expandmacular dystrophy, fenestrated sheen type ()
..expandmacular dystrophy, retinal, 3 ()
..expandmacular dystrophy, X-linked ()
..expandoccult macular dystrophy ()
..expandpatterned dystrophy of the retinal pigment epithelium ()
..expandretinal macular dystrophy type 2 ()
..expandunclassified primitive or secondary maculopathy ()
..expandvitelliform macular dystrophy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:20244
Name:unclassified primitive or secondary maculopathy
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal