Disease #05740 (XLID103 (intellectual developmental disorder, X-linked, type 103), OMIM:300982)

Official abbreviation XLID103
Name intellectual developmental disorder, X-linked, type 103
OMIM ID 300982
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene KLHL15
Associated tissues -
Disease features -
Remarks -
Date created 2020-05-11 15:12:58 +02:00 (CEST)
Date last edited 2023-10-23 16:36:10 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00385982 167926 - - M ? Germany - - - - - XLID103 Global developmental delay, Delayed speech and language development, Strabismus, Microcephaly, Constipation, Decreased small intestinal mucosa lactase level, Equinus calcaneus KLHL15 KLHL15 1 1 Andreas Laner
00438747 273182 - - M ? Turkey - - - - - XLID103 Atypical behavior, Delayed speech and language development, Abnormality of skin pigmentation, Intellectual disability, Neurodevelopmental delay KLHL15 KLHL15 1 1 Andreas Laner
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