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expandautosomal recessive cerebellar ataxia due to a DNA repair defect (MONDO:0020045)
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expandgenetic photodermatosis (MONDO:0015951)
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expandmalformation syndrome with skin/mucosae involvement (MONDO:0015331)
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expandpolymalformative genetic syndrome with increased risk of developing cancer (MONDO:0015945)
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expandprogeroid syndrome (MONDO:0015333)
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expandrare photodermatosis (MONDO:0019304)
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expandsyndromic retinitis pigmentosa (MONDO:0020240)
..Starting node
..expandxeroderma pigmentosum-Cockayne syndrome complex ()

       Child Nodes:
........expandxeroderma pigmentosum group B ()
........expandxeroderma pigmentosum group D ()
........expandxeroderma pigmentosum group F ()
........expandxeroderma pigmentosum group G ()



 Sister Nodes: 
..expandAlstrom syndrome ()
..expandautosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome ()
..expandBardet-Biedl syndrome ()
..expandcleft lip-retinopathy syndrome ()
..expandCockayne syndrome ()
..expandCohen syndrome ()
..expandfamilial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome ()
..expandhypogonadotropic hypogonadism-retinitis pigmentosa syndrome ()
..expandJoubert syndrome with ocular defect ()
..expandJoubert syndrome with oculorenal defect ()
..expandKearns-Sayre syndrome ()  LSDB  L: 00143;
..expandLaurence-Moon syndrome ()
..expandmuscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome ()
..expandoculotrichodysplasia ()
..expandosteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome ()
..expandpantothenate kinase-associated neurodegeneration ()
..expandPHARC syndrome ()
..expandprimary ciliary dyskinesia-retinitis pigmentosa syndrome ()
..expandpseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa ()
..expandretinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome ()
..expandretinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome ()
..expandretinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome ()
..expandRHYNS syndrome ()
..expandSaldino-Mainzer syndrome ()
..expandspastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome ()
..expandTELO2-related intellectual disability-neurodevelopmental disorder ()
..expandUsher syndrome ()
..expandxeroderma pigmentosum-Cockayne syndrome complex ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:16354
Name:xeroderma pigmentosum-Cockayne syndrome complex
Definition:Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) (see this term) together with the systemic and neurological features of Cockayne syndrome (CS; see this term).
Alternative IDs:
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Synonyms:XP/CS complex
Slim Mappings:
Reference: MedGen:
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OMIM:
MSeqDR LSDB:  
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