Sparse and thin eyebrow
Symptom Information:
Symptom ID: | HPO:0000535 | |||||||||||||||
Synonyms: |
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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 face(HPO:0000271) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) MedDRA: |
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Database Frequency: | 76 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
AREDYLD syndrome | (Orphanet:1133) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Barber-Say syndrome | (Orphanet:1231) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CEREBELLOFACIODENTAL SYNDROME | (OMIM:616202) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
DK1-CDG | (Orphanet:91131) |
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE | (OMIM:614929) |
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET | (OMIM:129540) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609944) |
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) |
Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
HYPOTRICHOSIS 6 | (OMIM:607903) |
HYPOTRICHOSIS 7 | (OMIM:604379) |
HYPOTRICHOSIS 8 | (OMIM:278150) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hyperlysinemia, type I | (OMIM:238700) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
Hypotrichosis simplex | (Orphanet:55654) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
KABUKI SYNDROME 1 | (OMIM:147920) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
KID syndrome | (Orphanet:477) |
Kabuki syndrome | (Orphanet:2322) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
MACS syndrome | (Orphanet:217335) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
Marie Unna hereditary hypotrichosis | (Orphanet:444) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Mucolipidosis type 2 | (Orphanet:576) |
NOONAN SYNDROME 4 | (OMIM:610733) |
Naxos disease | (Orphanet:34217) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
Netherton syndrome | (Orphanet:634) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
PACHYONYCHIA CONGENITA 2 | (OMIM:167210) |
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR | (OMIM:616099) |
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome | (Orphanet:276432) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES | (OMIM:615789) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
STORM SYNDROME | (OMIM:185069) |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome | (Orphanet:293165) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Tetrasomy 12p | (Orphanet:884) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
Yunis-Varon syndrome | (Orphanet:3472) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |