| Disease Browser
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Parent Node:
 developmental defect during embryogenesis (MONDO:0019755) |
..Starting node
.. branchial arch or oral-acral syndrome ()
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Child Nodes:
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| ........22q11.2 deletion syndrome () |
| ........acrofacial dysostosis Rodriguez type () |
| ........acrofacial dysostosis, Catania type () |
| ........acrofacial dysostosis, Kennedy-Teebi type () |
| ........acrofacial dysostosis, Palagonia type () |
| ........acrofacial dysostosis, Weyers type () |
| ........auriculocondylar syndrome () |
| ........branchio-oto-renal syndrome () |
| ........Charlie M syndrome () |
| ........epibulbar lipodermoid-preauricular appendage-polythelia syndrome () |
| ........frontofacionasal dysplasia () |
| ........frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome () |
| ........hypertelorism, microtia, facial clefting syndrome () |
| ........hypoglossia-hypodactyly syndrome () |
| ........Lambert syndrome () |
| ........mandibulofacial dysostosis-macroblepharon-macrostomia syndrome () |
| ........mandibulofacial dysostosis-microcephaly syndrome () |
| ........Meier-Gorlin syndrome () |
| ........Mobius syndrome () |
| ........Nager acrofacial dysostosis () |
| ........oculoauriculovertebral spectrum with radial defects () |
| ........orofaciodigital syndrome () |
| ........otofaciocervical syndrome () |
| ........otopalatodigital syndrome () |
| ........Patterson-Stevenson-Fontaine syndrome () |
| ........postaxial acrofacial dysostosis () |
| ........splenogonadal fusion-limb defects-micrognathia syndrome () |
| ........Townes-Brocks syndrome () |
| ........Treacher-Collins syndrome () |
| ........Wildervanck syndrome () |
| ........X-linked mandibulofacial dysostosis () |
Sister Nodes: |
..branchial arch or oral-acral syndrome ()
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..central nervous system malformation ()
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..chromosomal anomaly ()
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..congenital anomaly of kidney and urinary tract ()
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..congenital limb malformation ()
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..cranial malformation ()
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..developmental anomaly of metabolic origin ()
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..developmental defect of the eye ()
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..diaphragmatic or abdominal wall malformation ()
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..digestive tract malformation ()
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..hydrops fetalis (disease) ()
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..malformation syndrome with hamartosis ()
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..malformation syndrome with odontal and/or periodontal component ()
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..malformation syndrome with short stature ()
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..malformation syndrome with skin/mucosae involvement ()
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..multiple congenital anomalies/dysmorphic syndrome ()
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..overgrowth/obesity syndrome ()
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..progeroid syndrome ()
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..rare developmental defect with connective tissue involvement ()
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..rare head and neck malformation ()
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..rare teratologic disease ()
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..respiratory or mediastinal malformation ()
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..sex differentiation disease ()
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..syndromic genetic deafness ()
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..urogenital tract malformation ()
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..visceral malformation of the liver, biliary tract, pancreas or spleen ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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