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2013 MeSH

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Thanatophoric Dysplasia
MeSH HeadingThanatophoric Dysplasia
Tree NumberC05.116.099.343.110.500
Tree NumberC05.116.099.708.017.500
Tree NumberC05.660.585.984
Tree NumberC16.131.621.585.984
Tree NumberC16.320.240.500.500
Tree NumberC16.614.890
Scope NoteA severe form of neonatal dwarfism with very short limbs. All cases have died at birth or later in the neonatal period.
Entry TermDwarfism, Thanatophoric
Entry TermThanatophoric Dwarfism
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Previous Indexing Dwarfism (1966-1984)
Previous Indexing Skull (1966-1984)
History Note91(85); was see under OSTEOCHONDRODYSPLASIAS 1985-90
Date of Entry19840406
Unique IDD013796


MeSH Tree Structures

 
Musculoskeletal Diseases [C05]
   Bone Diseases [C05.116]
      Bone Diseases, Developmental [C05.116.099]
         Dwarfism [C05.116.099.343]
            Achondroplasia [C05.116.099.343.110]
Arrow pointing to current tree nodeThanatophoric Dysplasia [C05.116.099.343.110.500]

 
Musculoskeletal Diseases [C05]
   Bone Diseases [C05.116]
      Bone Diseases, Developmental [C05.116.099]
         Osteochondrodysplasias [C05.116.099.708]
            Achondroplasia [C05.116.099.708.017]
Arrow pointing to current tree nodeThanatophoric Dysplasia [C05.116.099.708.017.500]

 
Musculoskeletal Diseases [C05]
   Musculoskeletal Abnormalities [C05.660]
      Limb Deformities, Congenital [C05.660.585]
Arachnodactyly [C05.660.585.174]
Brachydactyly [C05.660.585.262]
Ectromelia [C05.660.585.350]
Lower Extremity Deformities, Congenital [C05.660.585.512]  +
Polydactyly [C05.660.585.600]  +
Proteus Syndrome [C05.660.585.620]
Syndactyly [C05.660.585.800]  +
Arrow pointing to current tree nodeThanatophoric Dysplasia [C05.660.585.984]
Upper Extremity Deformities, Congenital [C05.660.585.988]  +

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Musculoskeletal Abnormalities [C16.131.621]
         Limb Deformities, Congenital [C16.131.621.585]
Arachnodactyly [C16.131.621.585.174]
Brachydactyly [C16.131.621.585.262]
Ectromelia [C16.131.621.585.350]
Foot Deformities, Congenital [C16.131.621.585.380]  +
Hand Deformities, Congenital [C16.131.621.585.425]
Lower Extremity Deformities, Congenital [C16.131.621.585.512]
Polydactyly [C16.131.621.585.600]  +
Proteus Syndrome [C16.131.621.585.620]
Syndactyly [C16.131.621.585.800]  +
Arrow pointing to current tree nodeThanatophoric Dysplasia [C16.131.621.585.984]
Upper Extremity Deformities, Congenital [C16.131.621.585.988]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Dwarfism [C16.320.240]
         Achondroplasia [C16.320.240.500]
Arrow pointing to current tree nodeThanatophoric Dysplasia [C16.320.240.500.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]  +
Asphyxia Neonatorum [C16.614.092]
Birth Injuries [C16.614.131]  +
Congenital Hyperinsulinism [C16.614.200]  +
Cystic Fibrosis [C16.614.213]
Epilepsy, Benign Neonatal [C16.614.258]
Erythroblastosis, Fetal [C16.614.304]  +
Hernia, Umbilical [C16.614.378]
Hydrophthalmos [C16.614.438]
Hyperbilirubinemia, Neonatal [C16.614.451]  +
Hyperostosis, Cortical, Congenital [C16.614.465]
Ichthyosis [C16.614.492]  +
Infant, Premature, Diseases [C16.614.521]  +
Meconium Aspiration Syndrome [C16.614.580]
Mobius Syndrome [C16.614.595]
Neonatal Abstinence Syndrome [C16.614.610]
Nystagmus, Congenital [C16.614.643]
Ophthalmia Neonatorum [C16.614.677]
Persistent Fetal Circulation Syndrome [C16.614.694]
Rothmund-Thomson Syndrome [C16.614.760]
Sclerema Neonatorum [C16.614.810]
Severe Combined Immunodeficiency [C16.614.815]  +
Syphilis, Congenital [C16.614.868]
Arrow pointing to current tree nodeThanatophoric Dysplasia [C16.614.890]
Thrombocytopenia, Neonatal Alloimmune [C16.614.899]
Toxoplasmosis, Congenital [C16.614.909]
Vitamin K Deficiency Bleeding [C16.614.940]
Wolman Disease [C16.614.947]

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