Disease #00304 (ANPH (anencephaly (ANPH)), OMIM:206500)

Official abbreviation ANPH
Name anencephaly (ANPH)
OMIM ID 206500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene KIF7
Associated tissues -
Disease features -
Remarks -
Date created 2014-01-19 12:24:15 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00004256 - PubMed: Putoux 2011 consanguineous family ? yes Algeria - - - - - ANPH Corpus callosum: ?; Upper limb polydactyly: postaxial right; lower limb polydactyly: preaxial right and left; cleft palate; hallux duplication KIF7 KIF7 2 4 Tania Attie-Bitach
00004257 - PubMed: Putoux 2011 consanguineous family ? yes Algeria - - - - - ANPH Vermis: ?; Corpus callosum: ?; Cleft: ?; Hallux duplication KIF7 KIF7 2 4 Tania Attie-Bitach
00108623 - EJHG, submitted recurrent anencephaly, two fetuses to the same parents F no United States - - - - - ANPH Ultrasound at 18 weeks gestation showed anencephaly. The fetus had holoanencephaly, spinal rachischisis extending from the cervical to the sacral spine, a ventriculoseptal defect, absent brachiocephalic artery, origination of the right subclavian artery from the descending aorta, rocker bottom feet, and indeterminate genitalia. Multiple vertebral segmentation anomalies were present in the cervical and thoracic spine. The ribs were thin, and numbered nine on the left side and eleven on the right - CASP9 2 2 Michael Friez
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