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PrefixNamespace IRI
n12http://caligraph.org/ontology/ICD-9_code_240%E2%80%93279:_endocrine,_nutritional_and_metabolic_diseases,
n17http://en.wikipedia.org/wiki/List_of_ICD-9_codes_240%E2%80%93279:_endocrine,_nutritional_and_metabolic_diseases,
n11http://en.wikipedia.org/wiki/Category:
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Subject Item
clgr:Congenital_hypothyroidism
rdf:type
n6: n12:_and_immunity_disorders clgo:Disorder_included_in_newborn_screening_programs n16: clgo:Congenital_disorder_of_endocrine_system clgo:Cell_surface_receptor_deficiency owl:NamedIndividual
rdfs:label
Congenital hypothyroidism
owl:sameAs
dbr:Congenital_hypothyroidism
prov:wasDerivedFrom
n4:Chromosome_2 n4:Chromosome_1 n4:Goitre n4:List_of_disorders_included_in_newborn_screening_programs n4:Fontanelle n4:Global_developmental_delay n10: n4:Hypothyroidism n11:Congenital_disorders_of_endocrine_system n11:Cell_surface_receptor_deficiencies n13: n4:Chromosome_19 n14: n4:Chromosome_8 n17:_and_immunity_disorders n4:Chromosome_14 n4:Liotrix n4:Coarse_facial_features n4:Thyroid_disease
skos:prefLabel
Congenital hypothyroidism
skos:altLabel
Neonatal hypothyroidism congenital congenital cretinism hypothyroidism congenital hypothyroidism a lack of a functioning thyroid at birth
clgo:diseasesDB
6612
clgo:icd10
E00. E03.1 E03.0 ,
clgo:icd9
243
clgo:medlinePlus
001193
clgo:meshId
D003409
clgo:picture
clgr:Neonatal_jaundice