Carbohydrate metabolism
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Lipid/glycolipid metabolism
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Nucleotide metabolism
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Amino acid metabolism
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Glycan/glycoprotein metabolism
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Cofactor/vitamin metabolism
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Replication and repair
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nt06509 DNA replication
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H02569 Pulmonary fibrosis and/or bone marrow failure, telomere-related
H02525 Disorders of innate immunity
H00093 Combined immunodeficiency
H00094 Immunodeficiency associated with DNA repair defects
H02014 Ataxia-telangiectasia-like syndrome
H02031 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
H00290 Aicardi-Goutieres syndrome
H02484 X-linked reticulate pigmentary disorder with systemic manifestations
H00658 X-linked syndromic intellectual developmental disorder
H02342 Frontotemporal dementia and amyotrophic lateral sclerosis
H00264 Charcot-Marie-Tooth disease
H01118 Progressive external ophthalmoplegia
H00604 Deafness, autosomal dominant
H00564 Primary ciliary dyskinesia
H02366 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
H00992 Seckel syndrome
H01993 Baller-Gerold syndrome
H01889 Meier-Gorlin syndrome
H01734 Rothmund-Thomson syndrome
H00965 RAPADILINO syndrome
H02369 IMAGE-I syndrome
H02370 FILS syndrome
H02625 Primordial dwarfism-immunodeficiency-lipodystrophy syndrome
H01623 MDPL syndrome
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nt06510 Telomere length regulation
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nt06504 Base excision repair
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H00018 Gastric cancer
H02568 Polymerase proofreading-associated polyposis
H00021 Renal cell carcinoma
H01025 Familial adenomatous polyposis
H02624 Tumor predisposition syndrome
H00086 Hyper IgM syndromes, autosomal recessive type
H00094 Immunodeficiency associated with DNA repair defects
H00469 Mitochondrial DNA depletion syndrome
H01390 Mitochondrial neurogastrointestinal encephalomyopathy
H01891 Autosomal recessive spinocerebellar ataxias
H02573 Autosomal recessive spinocerebellar ataxias with axonal neuropathy
H00848 Ataxia with ocular apraxia
H02572 Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
H01118 Progressive external ophthalmoplegia
H02366 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
H02369 IMAGE-I syndrome
H02370 FILS syndrome
H01623 MDPL syndrome
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nt06502 Nucleotide excision repair
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nt06503 Mismatch repair
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nt06506 Double-strand break repair
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H00005 Chronic lymphocytic leukemia
H02418 Non-Hodgkin lymphoma
H00019 Pancreatic cancer
H00038 Melanoma
H00031 Breast cancer
H02531 Familial breast-ovarian cancer
H01132 Aplastic anemia
H00238 Fanconi anemia
H00507 Dyskeratosis congenita
H02569 Pulmonary fibrosis and/or bone marrow failure, telomere-related
H00092 T-B-Severe combined immunodeficiency
H01244 T+B+Severe combined immunodeficiencies (SCIDs)
H02554 Omenn syndrome
H00924 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation
H02015 LIG4 syndrome
H00064 Ataxia telangiectasia
H00094 Immunodeficiency associated with DNA repair defects
H00962 RIDDLE syndrome
H01344 Nijmegen breakage syndrome
H01346 Bloom syndrome
H02014 Ataxia-telangiectasia-like syndrome
H00768 Autosomal recessive intellectual developmental disorder
H01395 Autosomal recessive progressive external ophthalmoplegia
H00604 Deafness, autosomal dominant
H00627 Premature ovarian failure
H02492 Microcephaly, growth restriction, and increased sister chromatid exchange
H00992 Seckel syndrome
H01889 Meier-Gorlin syndrome
H01733 Werner syndrome
H02576 Familial cutaneous telangiectasia and cancer syndrome
H02578 Short stature, microcephaly, and endocrine dysfunction
H02639 Atelis syndrome
H01623 MDPL syndrome
H00296 Defects in RecQ helicases
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nt06508 Interstrand crosslink repair
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Signal transduction
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Cellular process
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Immune system
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Endocrine system
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