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Generalized Hypertrichosis Terminalis, with or without Gingival Hyperplasia (DOID:9006967)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
hypertrichosis +     
16Q24.3 Microdeletion Syndrome  
7p2 Monosomy Syndrome 
Acromegaloid Facial Appearance Syndrome 
Amaurosis Hypertrichosis  
Ambras type hypertrichosis universalis congenita 
autosomal dominant non-syndromic intellectual disability 22  
Barber-Say syndrome  
CAHMR Syndrome 
Cervical Hypertrichosis Neuropathy 
Cervical Hypertrichosis with Underlying Kyphoscoliosis 
chromosomal deletion syndrome +   
Chromosome 1, Deletion q21 q25 
Chromosome 1, Monosomy 1p 
Chromosome 1, Monosomy 1p22 p13 
Chromosome 1, Monosomy 1p31 p22 
Chromosome 1, Monosomy 1p32 
Chromosome 1, Monosomy 1p34 p32 
Chromosome 1, Monosomy 1q25 q32 
Chromosome 1, Monosomy 1q32 q42 
Chromosome 1, Monosomy 1q4 
Chromosome 10, Monosomy 10q 
Chromosome 11, Deletion 11p 
Chromosome 11p, Partial Deletion 
Chromosome 11q Partial Deletion 
Chromosome 12p Deletion 
Chromosome 12p Partial Deletion 
Chromosome 13q Deletion Syndrome +   
Chromosome 14q, Partial Deletions 
Chromosome 14q, Terminal Deletion 
Chromosome 15q, partial deletion 
Chromosome 17, Deletion 17q23 q24 
Chromosome 18, Deletion 18q23 
Chromosome 2, Monosomy 2p22 
Chromosome 2, Monosomy 2pter p24 
Chromosome 2, Monosomy 2q 
Chromosome 2, Monosomy 2q24 
Chromosome 20, deletion 20p 
Chromosome 21 Monosomy 
Chromosome 21, Monosomy 21q22 
Chromosome 22, Microdeletion 22 q11 
Chromosome 3, Monosomy 3p 
Chromosome 3, Monosomy 3p14 p11 
Chromosome 3, Monosomy 3p2 
Chromosome 3, Monosomy 3p25  
Chromosome 3, Monosomy 3q21 23 
Chromosome 3, Monosomy 3q27 
Chromosome 4 Short Arm Deletion 
Chromosome 4, 4q Terminal Deletion Syndrome 
Chromosome 4, Monosomy 4p14 p16 
Chromosome 4, Monosomy 4q32 
Chromosome 4q- Syndrome 
Chromosome 6, Deletion 6q13 q15 
Chromosome 6, Monosomy 6p23 
Chromosome 6, Monosomy 6q 
Chromosome 6, Monosomy 6q1 
Chromosome 6, monosomy 6q2 
Chromosome 7, Monosomy 
Chromosome 7, Monosomy 7q2 
Chromosome 7, Monosomy 7q21 
Chromosome 7, monosomy 7q3 
Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB 
Chromosome 8 Deletion +  
Chromosome 8, Monosomy 8p 
Chromosome 8, Monosomy 8p23 1 
Chromosome 8, Monosomy 8q 
Chromosome 8p Deletion Syndrome (partial) 
Chromosome 9, Partial Monosomy 9p 
Coffin-Siris syndrome +   
Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy 
Congenital Hypertrichosis Lanuginosa 
Deletion 13q Syndrome, Partial 
Deletion 6q16 q21 
Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome  
Facial Hypertrichosis  
Fragile Site 16p12 
Generalized Hypertrichosis Terminalis, with or without Gingival Hyperplasia  
Gingival Fibromatosis 1  
Gingival Fibromatosis 2 
Gingival Fibromatosis 3 
Gingival Fibromatosis 4 
gingival fibromatosis 5  
Gingival Fibromatosis with Distinctive Facies 
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Gorlin Chaudhry Moss Syndrome 
Hairy Ears 
Hairy Ears, Y-Linked 
Hairy Elbows 
Hairy Nose Tip 
Hypertrichosis Congenital Generalized X-Linked 
hypertrichosis of eyelid 
Hypertrichosis, Anterior Cervical 
hypertrichotic osteochondrodysplasia Cantu type  
Jones Syndrome 
Male Sterility due to Y-Chromosome Deletions 
Midphalangeal Hair 
Muller Barth Menger Syndrome 
Oliver-McFarlane syndrome  
Otodental Dysplasia 
Prader-Willi-Like Syndrome Associated with Chromosome 6 
Ramon Syndrome 
Schaap Taylor Baraitser Syndrome 
Sensorineural Deafness and Male Infertility  
Wiedemann Grosse Dibbern Syndrome 
X Chromosome, Monosomy Xp22 pter 
X Chromosome, Monosomy Xq28 
Zimmerman Laband Syndrome +   

Exact Synonyms: CHROMOSOME 17q24.2-q24.3 DUPLICATION SYNDROME ;   Chromosome 17q24.2-q24.3 Deletion Syndrome ;   Fibromatosis, Gingival, with Hypertrichosis ;   HTC3 ;   HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA ;   MICRODUPLICATION 17q24.2-q24.3 SYNDROME ;   Microdeletion 17q24.2-q24.3 Syndrome
Primary IDs: MESH:C565016
Alternate IDs: OMIM:135400

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