Disease #02037 (SMDP1 (surfactant metabolism dysfunction, pulmonary, type 1 (SMDP-1)), OMIM:265120)

Official abbreviation SMDP1
Name surfactant metabolism dysfunction, pulmonary, type 1 (SMDP-1)
OMIM ID 265120
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SFTPB
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

2 entries on 1 page. Showing entries 1 - 2.
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00435123 father Accepted manuscript in European Journal of Human Genetics - M yes France - >59y - - - SMDP1 - SFTPB SFTPB 1 2 Marie Legendre
00435124 - Accepted manuscript in European Journal of Human Genetics Son of 17GM02222 (individual 00435123) M yes France - >26y - - - SMDP1 - SFTPB SFTPB 1 1 Marie Legendre
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