Sparse hair
Symptom Information:
Symptom ID: | HPO:0008070 | |||||||||||||
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 density(HPO:0011357) Sparse hair(HPO:0008070) MedDRA: |
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Database Frequency: | 94 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
5p13 microduplication syndrome | (Orphanet:329802) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
ANGIOMA SERPIGINOSUM, X-LINKED | (OMIM:300652) |
AREDYLD syndrome | (Orphanet:1133) |
Acro-osteolysis-keloid-like lesions-premature aging syndrome | (Orphanet:363665) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant chondrodysplasia punctata | (Orphanet:79344) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
CARDIOFACIOCUTANEOUS SYNDROME 2 | (OMIM:615278) |
CEREBELLOFACIODENTAL SYNDROME | (OMIM:616202) |
COCKAYNE SYNDROME A | (OMIM:216400) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Coats plus syndrome | (Orphanet:313838) |
Cockayne syndrome | (Orphanet:191) |
Costello syndrome | (Orphanet:3071) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cranioectodermal dysplasia 2 | (OMIM:613610) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
De Barsy syndrome | (Orphanet:2962) |
Dyskeratosis congenita | (Orphanet:1775) |
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT | (OMIM:614940) |
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:614941) |
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 | (OMIM:615349) |
Ectodermal dysplasia - blindness | (Orphanet:1806) |
Filippi syndrome | (Orphanet:3255) |
Focal dermal hypoplasia | (Orphanet:2092) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hypodontia - dysplasia of nails | (Orphanet:2228) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
Incontinentia pigmenti | (Orphanet:464) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Loose anagen syndrome | (Orphanet:168) |
Lysinuric protein intolerance | (Orphanet:470) |
MACS syndrome | (Orphanet:217335) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 | (OMIM:614608) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 | (OMIM:615074) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM | (OMIM:606242) |
MGAT2-CDG | (Orphanet:79329) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
McDonough syndrome | (Orphanet:2471) |
Menkes disease | (Orphanet:565) |
Moynahan syndrome | (Orphanet:2574) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Myhre syndrome | (Orphanet:2588) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR | (OMIM:164680) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES | (OMIM:602249) |
PYCR1-related DeBarsy syndrome | (Orphanet:293633) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
ROBERTS SYNDROME | (OMIM:268300) |
Renpenning syndrome | (Orphanet:3242) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
Roberts syndrome | (Orphanet:3103) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |
SCARF syndrome | (Orphanet:3134) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Syndromic diarrhea | (Orphanet:84064) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE III | (OMIM:190351) |
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 | (OMIM:234050) |
Taurodontia - absent teeth - sparse hair | (Orphanet:2731) |
Trichodental syndrome | (Orphanet:3351) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Weaver syndrome | (Orphanet:3447) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
Wrinkly skin syndrome | (Orphanet:2834) |
Zunich-Kaye syndrome | (Orphanet:3474) |