Disease #01635 (AGOTC (agnathia-otocephaly complex), OMIM:202650)

Official abbreviation AGOTC
Name agnathia-otocephaly complex
OMIM ID 202650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00181105 - - - M no - - - - - - AGOTC Agnathia-otocephaly complex OTX2 OTX2 1 1 Isabel Filges
00181141 - Family 7, II.1 - M ? - - - - - - AGOTC Mandibular aplasia (HP:0009939), Microglossia (HP:0000171), Cleft palate (HP:0000175), Laryngeal hypoplasia (HP:0008749), Synotia (HP:0100663) SMAD3 SMAD3 1 1 Isabel Filges
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