Disease #01590 (TCMGLY (trichomegaly (TCMGLY)), OMIM:190330)

Official abbreviation TCMGLY
Name trichomegaly (TCMGLY)
OMIM ID 190330
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene FGF5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-10-18 21:28:12 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00385928 FamFT1 PubMed: Higgins 2014 7-generation family, 8 affected (3F, 5M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - TCMGLY excessively long eyelashes, no other ectodermal appendages, normal nails, normal teeth FGF5 FGF5 1 8 Johan den Dunnen
00385929 FamFT2 PubMed: Higgins 2014 2-generation family, 16 affected (7F, 9M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - TCMGLY excessively long eyelashes FGF5 FGF5 1 16 Johan den Dunnen
00385930 FamFT3 PubMed: Higgins 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Pakistan - - - - - TCMGLY - FGF5 FGF5 1 1 Johan den Dunnen
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