Sparse scalp hair
Symptom Information:
Symptom ID: | HPO:0002209 | ||||||||||||
Synonyms: |
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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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the scalp(HPO:0001965) Abnormality of the scalp hair(HPO:0100037) Sparse scalp hair(HPO:0002209) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of hair density(HPO:0011357) Sparse hair(HPO:0008070) Sparse scalp hair(HPO:0002209) Abnormality of the scalp hair(HPO:0100037) Sparse scalp hair(HPO:0002209) MedDRA: |
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Database Frequency: | 59 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
ADULT syndrome | (Orphanet:978) |
AREDYLD syndrome | (Orphanet:1133) |
Argininosuccinic aciduria | (Orphanet:23) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
Classical phenylketonuria | (Orphanet:79254) |
Coffin-Siris syndrome | (Orphanet:1465) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
DWARFISM, FAMILIAL, WITH MUSCLE SPASMS | (OMIM:600771) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Dubowitz syndrome | (Orphanet:235) |
ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE | (OMIM:614927) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Fried's tooth and nail syndrome | (Orphanet:99672) |
Genitopatellar syndrome | (Orphanet:85201) |
HYPOTRICHOSIS 8 | (OMIM:278150) |
Hawkinsinuria | (Orphanet:2118) |
Hereditary hypotrichosis with recurrent skin vesicles | (Orphanet:217407) |
Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Hypotrichosis simplex | (Orphanet:55654) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
LMNA-related cardiocutaneous progeria syndrome | (Orphanet:363618) |
Langer-Giedion syndrome | (Orphanet:502) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 | (OMIM:614607) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 | (OMIM:614609) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Menkes disease | (Orphanet:565) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Netherton syndrome | (Orphanet:634) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Oculotrichodysplasia | (Orphanet:2718) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Oligodontia - cancer predisposition syndrome | (Orphanet:300576) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR | (OMIM:616099) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Steinert myotonic dystrophy | (Orphanet:273) |
Transaldolase deficiency | (Orphanet:101028) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Werner syndrome | (Orphanet:902) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Wilson-Turner syndrome | (Orphanet:3459) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
Yunis-Varon syndrome | (Orphanet:3472) |