Low posterior hairline
Symptom Information:
Symptom ID: | HPO:0002162 | |||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the scalp(HPO:0001965) Abnormality of the scalp hair(HPO:0100037) Abnormality of the hairline(HPO:0009553) Low posterior hairline(HPO:0002162) Abnormality of the neck(HPO:0000464) Low posterior hairline(HPO:0002162) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the scalp hair(HPO:0100037) Abnormality of the hairline(HPO:0009553) Low posterior hairline(HPO:0002162) Abnormal hair pattern(HPO:0010720) Congenital abnormal hair pattern(HPO:0011361) Abnormality of the hairline(HPO:0009553) Low posterior hairline(HPO:0002162) MedDRA: |
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Database Frequency: | 88 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
3C syndrome | (Orphanet:7) |
3q29 microduplication | (Orphanet:251038) |
5p13 microduplication syndrome | (Orphanet:329802) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
BARAITSER-WINTER SYNDROME 1 | (OMIM:243310) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Camptodactyly - joint contractures - facial skeletal defects | (Orphanet:1323) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cataract - hypertrichosis - intellectual deficit | (Orphanet:1375) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cornelia de Lange syndrome | (Orphanet:199) |
Corpus callosum agenesis - double urinary collecting system | (Orphanet:1492) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 10q | (Orphanet:96148) |
Edinburgh malformation syndrome | (Orphanet:1895) |
Emery-Nelson syndrome | (Orphanet:1927) |
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS | (OMIM:227255) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Fetal hydantoin syndrome | (Orphanet:1912) |
Floating-Harbor syndrome | (Orphanet:2044) |
Glycogen storage disease due to aldolase A deficiency | (Orphanet:57) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Heart-hand syndrome type 2 | (Orphanet:1350) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Intellectual deficit, Wolff type | (Orphanet:3080) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
Intellectual deficit, X-linked, Siderius type | (Orphanet:85287) |
Isolated Klippel-Feil syndrome | (Orphanet:2345) |
Jung-Wolff-Back-Stahl syndrome | (Orphanet:2321) |
KBG syndrome | (Orphanet:2332) |
KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT | (OMIM:118100) |
KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE | (OMIM:214300) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Kousseff syndrome | (Orphanet:2351) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Lateral meningocele syndrome | (Orphanet:2789) |
Legius syndrome | (Orphanet:137605) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
MENTAL RETARDATION, X-LINKED 91 | (OMIM:300577) |
MURCS association | (Orphanet:2578) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
Monosomy 18p | (Orphanet:1598) |
Monosomy 9p | (Orphanet:261112) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
PTERYGIUM COLLI, ISOLATED | (OMIM:177990) |
Pachygyria - epilepsy - intellectual deficit - dysmorphism | (Orphanet:94084) |
Pilotto syndrome | (Orphanet:2894) |
Poland syndrome | (Orphanet:2911) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Prolidase deficiency | (Orphanet:742) |
Recombinant 8 syndrome | (Orphanet:96167) |
Ring chromosome 6 | (Orphanet:1448) |
Ring chromosome 8 | (Orphanet:1450) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SCARF syndrome | (Orphanet:3134) |
Shoulder and girdle defects - familial intellectual deficit | (Orphanet:2580) |
Sialuria | (Orphanet:3166) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloepimetaphyseal dysplasia, Geneviève type | (Orphanet:168454) |
Thoracomelic dysplasia | (Orphanet:1803) |
Trisomy 17p | (Orphanet:261290) |
Trisomy 20p | (Orphanet:261318) |
Turner syndrome | (Orphanet:881) |
Wildervanck syndrome | (Orphanet:3456) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |