Disease #07038 (HTC (hypertrichosis))

Official abbreviation HTC
Name hypertrichosis
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2023-11-01 15:17:13 +01:00 (CET)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00440336 FamPatII1 PubMed: DeStefano 2014 2-generation family, 1 affected, unaffected heterozygous parents/relatives F yes Yemen - - - - - HTC congenital generalized hypertrichosis terminalis, gingival hyperplasia, epilepsy; excessive hair growth face, forehead, cheeks, upper cutaneous lip, arms, upper and lower back and legs ABCA5 ABCA5, DGKZ, ZNF253 3 1 Johan den Dunnen
00440337 FamPatV2 PubMed: Raza 2022 5-generation family, 4 affected (4M), unaffected heterozygous parents/relatives F yes Pakistan - - - - - HTC see paper; ..., congenital hypertrichosis, excessive hair on arms, legs, scalp, face and back; gingival hyperplasia - ABCA5 1 4 Johan den Dunnen
00440338 FamPatV5 PubMed: Raza 2022 relative F yes Pakistan - - - - - HTC see paper; ..., 17y-deceased contracted chickenpox; congenital hypertrichosis entire body, gingival hyperplasia, epilepsy; EEG to diagnose epilepsy, following several fits - ABCA5 1 1 Johan den Dunnen
00440339 FamPatV6 PubMed: Raza 2022 relative F yes Pakistan - - - - - HTC see paper; ..., hypertrichosis, gingival hyperplasia, crowded teeth - ABCA5 1 1 Johan den Dunnen
00440340 FamPatV8 PubMed: Raza 2022 relative F yes Pakistan - - - - - HTC see paper; ..., congenital excessive hair growth head, arms, legs and back, gingival hyperplasia; mild congenital generalized hypertrichosis terminalissign - ABCA5 1 1 Johan den Dunnen
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