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- Meckel_syndrome abstract "Meckel syndrome (also known as Meckel–Gruber Syndrome, Gruber Syndrome, Dysencephalia Splanchnocystica) is a rare, lethal, ciliopathic, genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations (occipital encephalocele), polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios.Meckel–Gruber syndrome is named for Johann Meckel and Georg Gruber.".
- Meckel_syndrome diseasesdb "31661".
- Meckel_syndrome emedicineSubject "ped".
- Meckel_syndrome emedicineTopic "1390".
- Meckel_syndrome icd10 "Q61.9".
- Meckel_syndrome omim "249000".
- Meckel_syndrome thumbnail Autorecessive.svg?width=300.
- Meckel_syndrome wikiPageID "9446925".
- Meckel_syndrome wikiPageRevisionID "587821843".
- Meckel_syndrome diseasesdb "31661".
- Meckel_syndrome emedicinesubj "ped".
- Meckel_syndrome emedicinetopic "1390".
- Meckel_syndrome hasPhotoCollection Meckel_syndrome.
- Meckel_syndrome icd "Q61.9".
- Meckel_syndrome name "Meckel syndrome".
- Meckel_syndrome omim "249000".
- Meckel_syndrome wordnet_type synset-disease-noun-1.
- Meckel_syndrome subject Category:Autosomal_recessive_disorders.
- Meckel_syndrome subject Category:Ciliopathy.
- Meckel_syndrome subject Category:Congenital_disorders_of_urinary_system.
- Meckel_syndrome subject Category:Hepatology.
- Meckel_syndrome subject Category:Nephrology.
- Meckel_syndrome subject Category:Neurological_disorders.
- Meckel_syndrome subject Category:Rare_diseases.
- Meckel_syndrome type Abnormality114501726.
- Meckel_syndrome type Abstraction100002137.
- Meckel_syndrome type Anomaly114505821.
- Meckel_syndrome type Attribute100024264.
- Meckel_syndrome type AutosomalRecessiveDisorders.
- Meckel_syndrome type BirthDefect114465048.
- Meckel_syndrome type Condition113920835.
- Meckel_syndrome type CongenitalDisordersOfUrinarySystem.
- Meckel_syndrome type Defect114464005.
- Meckel_syndrome type Disease114070360.
- Meckel_syndrome type Disorder114052403.
- Meckel_syndrome type IllHealth114052046.
- Meckel_syndrome type Illness114061805.
- Meckel_syndrome type Imperfection114462666.
- Meckel_syndrome type NervousDisorder114084880.
- Meckel_syndrome type NeurologicalDisorders.
- Meckel_syndrome type PathologicalState114051917.
- Meckel_syndrome type PhysicalCondition114034177.
- Meckel_syndrome type State100024720.
- Meckel_syndrome type Disease.
- Meckel_syndrome type AilmentCondition.
- Meckel_syndrome type Situation.
- Meckel_syndrome comment "Meckel syndrome (also known as Meckel–Gruber Syndrome, Gruber Syndrome, Dysencephalia Splanchnocystica) is a rare, lethal, ciliopathic, genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations (occipital encephalocele), polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios.Meckel–Gruber syndrome is named for Johann Meckel and Georg Gruber.".
- Meckel_syndrome label "Meckel syndrome".
- Meckel_syndrome label "Meckel-Syndrom".
- Meckel_syndrome label "Syndrome de Meckel".
- Meckel_syndrome label "Síndrome de Meckel-Gruber".
- Meckel_syndrome label "Zespół Meckela".
- Meckel_syndrome label "Синдром Меккеля — Грубера".
- Meckel_syndrome sameAs Meckel-Syndrom.
- Meckel_syndrome sameAs Syndrome_de_Meckel.
- Meckel_syndrome sameAs Zespół_Meckela.
- Meckel_syndrome sameAs Síndrome_de_Meckel-Gruber.
- Meckel_syndrome sameAs m.02895yr.
- Meckel_syndrome sameAs Q1915681.
- Meckel_syndrome sameAs Q1915681.
- Meckel_syndrome sameAs 1034.
- Meckel_syndrome sameAs Meckel_syndrome.
- Meckel_syndrome wasDerivedFrom Meckel_syndrome?oldid=587821843.
- Meckel_syndrome depiction Autorecessive.svg.
- Meckel_syndrome isPrimaryTopicOf Meckel_syndrome.
- Meckel_syndrome name "Meckel syndrome".
