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  Diseases matching the query *Neonatal* and the corresponding human biomolecules involved in at least one interaction

Primary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00590607626Ichthyosis-sclerosing cholangitis neonatal syndrome1Show list of biomolecules +1
DI-02031610199Diabetes mellitus, neonatal, with congenital hypothyroidism1Show list of biomolecules +1
DI-02038300673Encephalopathy, neonatal severe, due to MECP2 mutations1Show list of biomolecules +1
DI-02039239200Hyperparathyroidism, neonatal severe1Show list of biomolecules +1
DI-02152606176Diabetes mellitus, permanent neonatal1Show list of biomolecules +1
DI-03171613977Cyanosis transient neonatal1Show list of biomolecules +1
DI-03306614328Inflammatory skin and bowel disease, neonatal, 11Show list of biomolecules +1
DI-03641608118Zinc deficiency, transient neonatal1Show list of biomolecules +1
DI-03858615371Pulmonary hypertension, neonatal1Show list of biomolecules +1
DI-04271616069Inflammatory skin and bowel disease, neonatal, 21Show list of biomolecules +1
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Secondary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00048202370Peroxisome biogenesis disorder 2B1Show list of biomolecules +1
DI-00136208085Arthrogryposis, renal dysfunction and cholestasis syndrome 11Show list of biomolecules +1
DI-00329607765Congenital bile acid synthesis defect 11Show list of biomolecules +1
DI-00440225400Ehlers-Danlos syndrome 61Show list of biomolecules +1
DI-00459609638Epidermolysis bullosa, lethal acantholytic1Show list of biomolecules +1
DI-00474612164Epileptic encephalopathy, early infantile, 41Show list of biomolecules +1
DI-00607609583Joubert syndrome 41Show list of biomolecules +1
DI-00699154700Marfan syndrome1Show list of biomolecules +1
DI-00922614886Peroxisome biogenesis disorder complementation group 141Show list of biomolecules +1
DI-00957612304Thrombophilia due to protein C deficiency, autosomal recessive1Show list of biomolecules +1
DI-00965266200Pyruvate kinase deficiency of red cells1Show list of biomolecules +1
DI-01103131705Transient bullous dermolysis of the newborn1Show list of biomolecules +1
DI-01144277610Weissenbacher-Zweymueller syndrome1Show list of biomolecules +1
DI-01149226980Wolcott-Rallison syndrome1Show list of biomolecules +1
DI-01181604131Alpha-thalassemia1Show list of biomolecules +1
DI-01224177735Pseudohypoaldosteronism 1, autosomal dominant1Show list of biomolecules +1
DI-01279264070Hyperphenylalaninemia, BH4-deficient, D1Show list of biomolecules +1
DI-01349607115Chronic infantile neurologic cutaneous and articular syndrome1Show list of biomolecules +1
DI-01356272430Cold-induced sweating syndrome 11Show list of biomolecules +1
DI-01357610313Cold-induced sweating syndrome 21Show list of biomolecules +1
DI-01367610678Combined oxidative phosphorylation deficiency 41Show list of biomolecules +1
DI-01385612540Myopathy, congenital, Compton-North1Show list of biomolecules +1
DI-01420610015Congenital systemic glutamine deficiency1Show list of biomolecules +1
DI-01469220110Mitochondrial complex IV deficiency3Show list of biomolecules +3
DI-01606228000Farber lipogranulomatosis1Show list of biomolecules +1
DI-01638606812Fumarase deficiency1Show list of biomolecules +1
DI-01745613711Hirschsprung disease 31Show list of biomolecules +1
DI-01746142623Hirschsprung disease 11Show list of biomolecules +1
DI-01747600155Hirschsprung disease 21Show list of biomolecules +1
DI-01811304790Immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome1Show list of biomolecules +1
DI-01894275210Lethal tight skin contracture syndrome1Show list of biomolecules +1
DI-01974251120Methylmalonyl-CoA epimerase deficiency1Show list of biomolecules +1
DI-01981252010Mitochondrial complex I deficiency4Show list of biomolecules +4
DI-02002255320Multiminicore disease with external ophthalmoplegia1Show list of biomolecules +1
DI-02080604901North American Indian childhood cirrhosis1Show list of biomolecules +1
DI-02165609049Pierson syndrome1Show list of biomolecules +1
DI-02244259775Raine syndrome1Show list of biomolecules +1
DI-02363187600Thanatophoric dysplasia 11Show list of biomolecules +1
DI-02790613454Rett syndrome congenital variant1Show list of biomolecules +1
DI-03018263520Short-rib thoracic dysplasia 6 with or without polydactyly1Show list of biomolecules +1
DI-03083613869Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related1Show list of biomolecules +1
DI-03093187601Thanatophoric dysplasia 21Show list of biomolecules +1
DI-03146614067Cerebral palsy, spastic quadriplegic 61Show list of biomolecules +1
DI-03152614081Anhaptoglobinemia1Show list of biomolecules +1
DI-03174613986Pituitary hormone deficiency, combined, 61Show list of biomolecules +1
DI-03203614080Multiple congenital anomalies-hypotonia-seizures syndrome 11Show list of biomolecules +1
DI-03305240900Hypoinsulinemic hypoglycemia with hemihypertrophy1Show list of biomolecules +1
DI-03365614514Thrombophilia due to protein S deficiency, autosomal recessive1Show list of biomolecules +1
DI-03400614524Fibrochondrogenesis 21Show list of biomolecules +1
DI-03403300868Multiple congenital anomalies-hypotonia-seizures syndrome 21Show list of biomolecules +1
DI-03405614501Psychomotor retardation, epilepsy, and craniofacial dysmorphism1Show list of biomolecules +1
DI-03461614653Neuropathy, hereditary sensory and autonomic, 61Show list of biomolecules +1
DI-03579214110Peroxisome biogenesis disorder 2A1Show list of biomolecules +1
DI-03595614886Peroxisome biogenesis disorder 12A1Show list of biomolecules +1
DI-03599614970Joubert syndrome 201Show list of biomolecules +1
DI-03630614946Combined oxidative phosphorylation deficiency 141Show list of biomolecules +1
DI-03664615006Epileptic encephalopathy, early infantile, 151Show list of biomolecules +1
DI-03710615182Combined D-2- and L-2-hydroxyglutaric aciduria1Show list of biomolecules +1
DI-03926615503Short-rib thoracic dysplasia 8 with or without polydactyly1Show list of biomolecules +1
DI-04078155310Visceral myopathy1Show list of biomolecules +1
DI-04118615824Mitochondrial complex III deficiency, nuclear 71Show list of biomolecules +1
DI-04167250220Spondylometaphyseal dysplasia, Sedaghatian type1Show list of biomolecules +1
DI-04246616050Autoinflammation with infantile enterocolitis1Show list of biomolecules +1
DI-04443616393Mental retardation, autosomal dominant 381Show list of biomolecules +1
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