| Disease Browser
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Parent Node:
 Craniofacial Abnormalities (D019465) |
Parent Node:
Dental Enamel Hypoplasia (D003744) |
Parent Node:
Hair Diseases (D006201) |
..Starting node
.. Tricho-dento-osseous syndrome (C536549)
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Child Nodes:
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Sister Nodes: |
..Bamforth syndrome (C537901)
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..Bird headed dwarfism Montreal type (C535448)
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..Bjornstad syndrome (C537633)
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..Cardiomyopathy dilated with Woolly hair and keratoderma (C535581)
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..Catatrichy (C535346)
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..Copper deficiency, familial benign (C535468)
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..Curly hair-ankyloblepharon-nail dysplasia syndrome (C538074)
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..Dermoodontodysplasia (C565103)
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..ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
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..FLOTCH syndrome (C537065)
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..Folliculitis (D005499)  2
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..Giedion syndrome (C536820)
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..Hairy palms and soles (C535620)
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..Hirsutism (D006628) 6
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..Hypertrichosis (D006983) 27
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..Hypotrichosis (D007039) 89
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..Kaler Garrity Stern syndrome (C537706)
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..Katsantoni Papadakou Lagoyanni syndrome (C537012)
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..Kozlowski-Krajewska syndrome (C537615)
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..Martinez Monasterio Pinheiro syndrome (C536027)
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..Menkes Kinky Hair Syndrome (D007706) 1
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..Monilethrix (D056734) 1
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..Naxos disease (C538346)
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..Oculotrichodysplasia (C564934)
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..Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
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..Piedra (D010854)
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..Pili annulati (C537187)
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..Pili multigemini (C537188)
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..Pili Torti (C562485)
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..Pili torti developmental delay neurological abnormalities (C537398)
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..Pili torti onychodysplasia (C537399)
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..Pseudofolliculitis Barbae (C563016)
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..Pseudomonilethrix (C562988)
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..Rodrigues blindness (C535865)
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..Skin Fragility-Woolly Hair Syndrome (C564359)
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..Trichilemmal Cyst 1 (C566458)
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..Tricho-dento-osseous syndrome (C536549)
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..Tricho-dento-osseous syndrome 1 (C536550)
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..TRICHODENTOOSSEOUS SYNDROME (OMIM:190320)
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..Trichodysplasia-Xeroderma (C566032)
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..Trichohepatoenteric Syndrome (C565627)
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..Trichorhinophalangeal Syndrome, Type III (C566033)
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..Trichostasis spinulosa (C536558)
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..TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675)
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..Uncombable hair syndrome (C536939)
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..White forelock with malformations (C536700)
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..WOOLLY HAIR, AUTOSOMAL DOMINANT (OMIM:194300)
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..Woolly Hair, Autosomal Recessive (C564735)
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..Woolly hair, congenital (C536745)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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