ONTOLOGY REPORT - ANNOTATIONS


Term:hypertrichosis
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Accession:DOID:420 term browser browse the term
Definition:Excessive hair growth at inappropriate locations, such as on the extremities, the head, and the back. It is caused by genetic or acquired factors, and is an androgen-independent process. This concept does not include HIRSUTISM which is an androgen-dependent excess hair growth in WOMEN and CHILDREN.
Synonyms:exact_synonym: Hypertrichoses
 primary_id: MESH:D006983;   RDO:0000294
 xref: ORDO:79365
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hypertrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arid1b AT-rich interaction domain 1B JBrowse link 1 45,923,119 46,232,301 RGD:8554872
G Asxl1 ASXL transcriptional regulator 1 JBrowse link 3 148,832,231 148,902,356 RGD:8554872
G Kcnj11 potassium voltage-gated channel subfamily J member 11 JBrowse link 1 102,103,093 102,107,134 RGD:8554872
G Naglu N-acetyl-alpha-glucosaminidase JBrowse link 10 88,979,363 88,986,879 RGD:8554872
G Slc29a3 solute carrier family 29 member 3 JBrowse link 20 30,289,527 30,327,343 RGD:11554173
Amaurosis Hypertrichosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cnnm4 cyclin and CBS domain divalent metal cation transport mediator 4 JBrowse link 9 43,049,587 43,088,690 RGD:11554173
Barber-Say syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Twist2 twist family bHLH transcription factor 2 JBrowse link 9 98,924,134 98,968,510 RGD:8554872
RGD:7240710
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abca5 ATP binding cassette subfamily A member 5 JBrowse link 10 98,573,226 98,645,028 RGD:8554872
RGD:7240710
hypertrichotic osteochondrodysplasia Cantu type term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcc9 ATP binding cassette subfamily C member 9 JBrowse link 4 176,806,098 176,928,540 RGD:7240710
RGD:8554872
RGD:11554173
G Kcnj8 potassium voltage-gated channel subfamily J member 8 JBrowse link 4 176,783,287 176,789,143 RGD:11554173
Oliver-McFarlane Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pnpla6 patatin-like phospholipase domain containing 6 JBrowse link 12 2,068,749 2,098,139 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      integumentary system disease 2253
        hair disease 204
          hypertrichosis 11
            Acromegaloid Facial Appearance Syndrome 0
            Amaurosis Hypertrichosis 1
            Ambras type hypertrichosis universalis congenita 0
            Barber-Say syndrome 1
            CAHMR Syndrome 0
            Cervical Hypertrichosis Neuropathy 0
            Cervical Hypertrichosis with Underlying Kyphoscoliosis 0
            Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy 0
            Congenital Hypertrichosis Lanuginosa 0
            Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome 0
            Facial Hypertrichosis 0
            Gingival Fibromatosis with Hypertrichosis and Mental Retardation 0
            Gorlin Chaudhry Moss Syndrome 0
            Hairy Ears 0
            Hairy Ears, Y-Linked 0
            Hairy Elbows 0
            Hairy Nose Tip 0
            Hypertrichosis Congenital Generalized X-Linked 0
            Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia 1
            Hypertrichosis, Anterior Cervical 0
            Hypertrichosis, Hyperkeratosis, Mental Retardation, and Distinctive Facial Features 0
            Midphalangeal Hair 0
            Muller Barth Menger Syndrome 0
            Oliver-McFarlane Syndrome 1
            Ramon Syndrome 0
            Schaap Taylor Baraitser Syndrome 0
            Wiedemann Grosse Dibbern Syndrome 0
            hypertrichosis of eyelid 0
            hypertrichotic osteochondrodysplasia Cantu type 2
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        sensory system disease 4246
          skin disease 2253
            hair disease 204
              hypertrichosis 11
                Acromegaloid Facial Appearance Syndrome 0
                Amaurosis Hypertrichosis 1
                Ambras type hypertrichosis universalis congenita 0
                Barber-Say syndrome 1
                CAHMR Syndrome 0
                Cervical Hypertrichosis Neuropathy 0
                Cervical Hypertrichosis with Underlying Kyphoscoliosis 0
                Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy 0
                Congenital Hypertrichosis Lanuginosa 0
                Facial Dysmorphism, Hypertrichosis, Epilepsy, Intellectual/Developmental Delay, and Gingival Overgrowth Syndrome 0
                Facial Hypertrichosis 0
                Gingival Fibromatosis with Hypertrichosis and Mental Retardation 0
                Gorlin Chaudhry Moss Syndrome 0
                Hairy Ears 0
                Hairy Ears, Y-Linked 0
                Hairy Elbows 0
                Hairy Nose Tip 0
                Hypertrichosis Congenital Generalized X-Linked 0
                Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia 1
                Hypertrichosis, Anterior Cervical 0
                Hypertrichosis, Hyperkeratosis, Mental Retardation, and Distinctive Facial Features 0
                Midphalangeal Hair 0
                Muller Barth Menger Syndrome 0
                Oliver-McFarlane Syndrome 1
                Ramon Syndrome 0
                Schaap Taylor Baraitser Syndrome 0
                Wiedemann Grosse Dibbern Syndrome 0
                hypertrichosis of eyelid 0
                hypertrichotic osteochondrodysplasia Cantu type 2
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.