Fine hair
Symptom Information:
Symptom ID: | HPO:0002213 | ||||
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) Fine hair(HPO:0002213) MedDRA: |
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Database Frequency: | 77 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT | (OMIM:101840) |
ADULT syndrome | (Orphanet:978) |
ANGIOMA SERPIGINOSUM, X-LINKED | (OMIM:300652) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Acrogeria | (Orphanet:2500) |
Acromelanosis | (Orphanet:39) |
Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
CARDIOFACIOCUTANEOUS SYNDROME 2 | (OMIM:615278) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Choroidal atrophy - alopecia | (Orphanet:1433) |
Cockayne syndrome | (Orphanet:191) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Crandall syndrome | (Orphanet:202) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Distal trisomy 6p | (Orphanet:1745) |
Dubowitz syndrome | (Orphanet:235) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia - blindness | (Orphanet:1806) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Genitopatellar syndrome | (Orphanet:85201) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hawkinsinuria | (Orphanet:2118) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hypodontia - dysplasia of nails | (Orphanet:2228) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Isolated sulfite oxidase deficiency | (Orphanet:99731) |
KID syndrome | (Orphanet:477) |
Lysinuric protein intolerance | (Orphanet:470) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Monilethrix | (Orphanet:573) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Myhre syndrome | (Orphanet:2588) |
Netherton syndrome | (Orphanet:634) |
Neuroectodermal-endocrine syndrome | (Orphanet:2676) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodentodigital dysplasia | (Orphanet:2710) |
PYCR1-related DeBarsy syndrome | (Orphanet:293633) |
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome | (Orphanet:276432) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
Ringed hair disease | (Orphanet:169) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
Syndromic diarrhea | (Orphanet:84064) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Trichodental syndrome | (Orphanet:3351) |
Trichodermal syndrome - intellectual deficit | (Orphanet:3360) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Weaver syndrome | (Orphanet:3447) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
Woolly hair | (Orphanet:170) |
Zunich-Kaye syndrome | (Orphanet:3474) |