Disease #03491 (FANCP (Fanconi anemia, complementation group P (FANCP)), OMIM:613951)

Official abbreviation FANCP
Name Fanconi anemia, complementation group P (FANCP)
OMIM ID 613951
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene SLX4
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

7 entries on 1 page. Showing entries 1 - 7.
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00020020 - PubMed: Stoepker 2011 - M ? - - - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020021 - PubMed: Stoepker 2011 - ? ? - - - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020022 - PubMed: Kim 2011 - F ? - South Indian - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020023 - PubMed: Kim 2011 - M ? - - - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020024 - PubMed: Stoepker 2011 - ? ? - - - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020025 - PubMed: Stoepker 2011 - ? ? - - - - - - FANCP - SLX4 SLX4 2 1 Arleen D. Auerbach
00020026 - Schuster et al, 2012 - F no - - - - - - FANCP prenatal dystrophy, short stature, hypoplasia right thumb, microcephaly, hyperpigmentation, cafÈ-au-lait, vitiligo, hypothyreoidism SLX4 SLX4 2 1 Beatrice Schuster
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