Disease #00452 (PSAPD (saposin deficiency, combined (PSAPD)), OMIM:611721)

Official abbreviation PSAPD
Name saposin deficiency, combined (PSAPD)
OMIM ID 611721
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 PSAP
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-09 21:23:07 +02:00 (CEST)
Date last edited 2021-06-30 08:22:28 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00017866 - PubMed: Kretz 1990, PubMed: Rafi 1990 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M ? United States - - - - - PSAPD HPLC analysis of normal and saposin B-deficient lymphoblasts showed no saposin A, C, or D deficiency PSAP PSAP 1 2 Johan den Dunnen
00080895 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - PSAPD Combined SAP deficiency (OMIM:611721) PSAP PSAP 1 1 Daniel Trujillano
00080920 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - PSAPD Combined SAP deficiency (OMIM:611721) PSAP PSAP 1 1 Daniel Trujillano
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