Phenotypes for disease #00336 (ARCND1 (auriculocondylar syndrome, type 1 (ARCND-1)), OMIM:602483)

6 entries on 1 page. Showing entries 1 - 6.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000014788 severe mandibular abnormalities, congenital mandibular ankylosis with lateral fusion mandible to temporozygomatic suture, medial fusion to skull base (medial and lateral pterygoid plates), resulting in airway obstruction requiring tracheostomy; severe microglossia, elongated soft-tissue masses attached at posterior floor mouth, excessive soft tissue protruding from medial alveolus lower jaw - - Familial, autosomal dominant - - - - - Johan den Dunnen 00016105
0000014789 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00016106
0000014795 - - - Familial, autosomal dominant - - - - - Maria Rita Passos-Bueno 00016123
0000014796 - - - Isolated (sporadic) - - - - - Maria Rita Passos-Bueno 00016124
0000014797 - - - Isolated (sporadic) - - - - - Maria Rita Passos-Bueno 00016125
0000014803 question mark ears, micro- and/or retrognathia, facial asymmetry; presented with asymmetric micrognathia, malocclusion, microstomia, notch between lobe and helix right ear; X-ray mildly hypoplastic first ribs - - Familial, autosomal dominant - - - - - Johan den Dunnen 00016207
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