Coarse hair
Symptom Information:
Symptom ID: | HPO:0002208 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of hair texture(HPO:0010719) Coarse hair(HPO:0002208) MedDRA: |
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Database Frequency: | 58 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acroosteolysis, dominant type | (Orphanet:955) |
Amaurosis - hypertrichosis | (Orphanet:1021) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Argininosuccinic aciduria | (Orphanet:23) |
Autosomal dominant chondrodysplasia punctata | (Orphanet:79344) |
Autosomal recessive cutis laxa type 2, classic type | (Orphanet:357074) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Björnstad syndrome | (Orphanet:123) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Brain malformation - congenital heart disease - postaxial polydactyly | (Orphanet:75389) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cohen syndrome | (Orphanet:193) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia - sensorineural deafness | (Orphanet:1883) |
Emery-Nelson syndrome | (Orphanet:1927) |
Fetal hydantoin syndrome | (Orphanet:1912) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
HYPOTRICHOSIS 8 | (OMIM:278150) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypotrichosis simplex | (Orphanet:55654) |
Incontinentia pigmenti | (Orphanet:464) |
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE | (OMIM:248010) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Marie Unna hereditary hypotrichosis | (Orphanet:444) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Multiple sulfatase deficiency | (Orphanet:585) |
Noonan syndrome | (Orphanet:648) |
ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR | (OMIM:164680) |
Occipital horn syndrome | (Orphanet:198) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Pili torti | (Orphanet:2889) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SENER SYNDROME | (OMIM:606156) |
Sanfilippo syndrome type A | (Orphanet:79269) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Sanfilippo syndrome type C | (Orphanet:79271) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Shoulder and girdle defects - familial intellectual deficit | (Orphanet:2580) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Uncombable hair syndrome | (Orphanet:1410) |
WOOLLY HAIR, AUTOSOMAL DOMINANT | (OMIM:194300) |
Woolly hair | (Orphanet:170) |