Disease #01715 (ACHM2 (achromatopsia, type 2 (ACHM-2)), OMIM:216900)

Official abbreviation ACHM2
Name achromatopsia, type 2 (ACHM-2)
OMIM ID 216900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene CNGA3
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

5 entries on 1 page. Showing entries 1 - 5.
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00382087 12 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ACHM2 microphthalmia, anophthalmia, and coloboma; MIM, 206920 SMOC1 SMOC1 2 1 LOVD
00382123 89 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ACHM2 retinal dystrophy; MIM, 216900 CNGA3 CNGA3 1 1 LOVD
00382124 268 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ACHM2 retinal dystrophy; MIM, 216900 CNGA3 CNGA3 2 1 LOVD
00382125 272 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ACHM2 retinal dystrophy; MIM, 216900 CNGA3 CNGA3 1 1 LOVD
00382126 278 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - ACHM2 retinal dystrophy; MIM, 216900 CNGA3 CNGA3 2 1 LOVD
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