Low posterior hairline

Symptom Information:

Symptom ID: HPO:0002162
Synonyms:
Low posterior hair line [HPO:0002162]
Low posterior hair line [OMIM:Low posterior hair line]
Low posterior hairline [OMIM:Low posterior hairline]
Low hair line (back) [Orphanet:24800]
Low hair line [OMIM:Low hair line]
Low posterior hairline (1 patient) [OMIM:Low posterior hairline (1 patient)]
Low posterior hairline (rare) [OMIM:Low posterior hairline (rare)]
Quality:
Cross references:
Orphanet:24800 "Low hair line (back)" [Orphanet:24800]
OMIM: "Low posterior hair line" [OMIM:Low posterior hair line]
OMIM: "Low posterior hairline" [OMIM:Low posterior hairline]
OMIM: "Low hair line" [OMIM:Low hair line]
OMIM: "Low posterior hairline (1 patient)" [OMIM:Low posterior hairline (1 patient)]
OMIM: "Low posterior hairline (rare)" [OMIM:Low posterior hairline (rare)]
Is a (Direct Parents):
HPO         Abnormality of the neck
HPO         Abnormality of the hairline
Orphanet Abnormality of the hairline
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)
                Abnormal hair pattern(HPO:0010720)
                   Congenital abnormal hair pattern(HPO:0011361)
                      Abnormality of the hairline(HPO:0009553)
                         Low posterior hairline(HPO:0002162)
                Abnormality of the scalp hair(HPO:0100037)
                   Abnormality of the hairline(HPO:0009553)
                      Low posterior hairline(HPO:0002162)
MedDRA:
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)