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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:developmental defect during embryogenesis
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Accession:EFO:MONDO:0019755 term browser browse the term
Definition:A disease that has its basis in the disruption of embryonic morphogenesis.
Synonyms:exact_synonym: NCIT:C99267;   Orphanet:93890;   congenital malformation syndrome;   disorder of embryonic morphogenesis;   embryonic morphogenesis disease;   http://identifiers.org/medgen/1825997;   http://identifiers.org/snomedct/400038003;   http://linkedlifedata.com/resource/umls/id/C5680284;   malformation syndrome;   rare developmental defect during embryogenesis
 alt_id: MONDO:0019755
 xref: ICD9:759.7;   MEDGEN:1825997;   NCI:C99267;   ORDO:93890;   SCTID:400038003;   UMLS:C5680284


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  experimental factor 0
    material property 0
      disposition 0
        disease 0
          disorder of development or morphogenesis 0
            developmental defect during embryogenesis 0
              Becker nevus syndrome + 0
              Desbuquois dysplasia + 0
              Ehlers-Danlos syndrome + 0
              Larsen syndrome 0
              Legius syndrome 0
              Maffucci syndrome 0
              PTEN hamartoma tumor syndrome + 0
              TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations + 0
              abdominal wall malformation + 0
              angioosteohypertrophic syndrome 0
              ankyloblepharon filiforme-imperforate anus syndrome 0
              anotia 0
              blindness - scoliosis - arachnodactyly syndrome 0
              bone fragility with contractures, arterial rupture, and deafness 0
              central nervous system malformation + 0
              cleft palate + 0
              congenital anomaly of kidney and urinary tract + 0
              congenital limb malformation + 0
              cutis laxa + 0
              cutis laxa - Marfanoid syndrome 0
              cysts and fistulae of the face and oral cavity + 0
              developmental anomaly of metabolic origin + 0
              developmental defect of the eye + 0
              digestive tract malformation + 0
              disorder of sexual differentiation + 0
              facial cleft + 0
              focal dermal hypoplasia 0
              hemihyperplasia-multiple lipomatosis syndrome 0
              hereditary hemorrhagic telangiectasia + 0
              hereditary neurocutaneous angioma 0
              hydrops fetalis + 0
              infectious embryofetopathy + 0
              joint laxity, short stature, and myopia 0
              lethal Larsen-like syndrome 0
              linear nevus sebaceous syndrome 0
              macroglossia + 0
              marfanoid habitus-inguinal hernia-advanced bone age syndrome 0
              microtia 0
              multiple congenital anomalies/dysmorphic syndrome + 0
              neurofibromatosis type 1 + 0
              neurofibromatosis-Noonan syndrome + 0
              nevoid basal cell carcinoma syndrome 0
              phakomatosis pigmentokeratotica 0
              phakomatosis pigmentovascularis + 0
              progeroid syndrome + 0
              pseudodiastrophic dysplasia 0
              schwannomatosis 0
              toxic or drug-related embryofetopathy + 0
              urogenital tract malformation + 0
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