Phenotypes for disease #01016 (AOS2 (Adams-Oliver syndrome, type 2 (AOS-2)), OMIM:614219)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000224155 no microcephaly (-HP000252), no scalp defects, no developmental delay, no dilatation - - Familial, X-linked recessive 00y08m 00y01m 00y01m - - Yan Cai 00296754
0000308705 microcephaly (<3rd centile, HP:0000252), aplasia cutis congenita scalp (HP:0007385), global developmental delay (HP:0001263) Adams-Oliver syndrome AOS2 Familial, autosomal recessive 02y 04y 00y - - Martin Zenker 00417195
0000335775 aplasia cutis congenita of the scalp (HP:0007385); hypertelorism (HP:0000316); vitreoretinal abnormalities, congenita (HP:0007773); cutis marmorata (HP:0000965); calcifications of cerebral ventricles - AOS2 Familial, autosomal recessive 17 01y02m 00y00m17d Congenital onset - Maria Elena García Paya 00446573
0000351752 Neurodevelopmental delay, Microcephaly, Abnormality of the distal phalanges of the toes, Abnormal distal phalanx morphology of finger, 2-3 toe syndactyly - - Familial, autosomal recessive 09y - - - - Andreas Laner 00466389
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