Tall stature

Symptom Information:

Symptom ID: HPO:0000098
Synonyms:
Accelerated linear growth [HPO:0000098]
Increased body height [HPO:0000098]
Increased linear growth [HPO:0000098]
Tall stature (finding) [Orphanet:53250]
Tall stature [Orphanet:53250]
Accelerated linear growth [OMIM:Accelerated linear growth]
Increased linear growth [OMIM:Increased linear growth]
Tall stature [OMIM:Tall stature]
Tall stature/gigantism/growth acceleration [Orphanet:53250]
Stature tall [Orphanet:53250]
Body height above normal [MedDRA:10056810]
Stature tall [MedDRA:10056810]
Accelerated linear growth (in 1 of 2 patients) [OMIM:Accelerated linear growth (in 1 of 2 patients)]
Tall stature (46%) [OMIM:Tall stature (46%)]
Tall stature (>97th centile) [OMIM:Tall stature (>97th centile)]
Tall stature (male mean adult height 195.6cm, female mean adult height 177.8cm) [OMIM:Tall stature (male mean adult height 195.6cm, female mean adult height 177.8cm)]
Gigantism [MedDRA:10018265]
Gigantism (disorder) [Orphanet:53250]
Gigantism [Orphanet:53250]
Body height increased [MedDRA:10056813]
Quality:
Cross references:
Orphanet:53250 "Tall stature/gigantism/growth acceleration" [Orphanet:53250]
OMIM: "Accelerated linear growth" [OMIM:Accelerated linear growth]
OMIM: "Increased linear growth" [OMIM:Increased linear growth]
OMIM: "Tall stature" [OMIM:Tall stature]
OMIM: "Accelerated linear growth (in 1 of 2 patients)" [OMIM:Accelerated linear growth (in 1 of 2 patients)]
OMIM: "Tall stature (46%)" [OMIM:Tall stature (46%)]
OMIM: "Tall stature (>97th centile)" [OMIM:Tall stature (>97th centile)]
OMIM: "Tall stature (male mean adult height 195.6cm, female mean adult height 177.8cm)" [OMIM:Tall stature (male mean adult height 195.6cm, female mean adult height 177.8cm)]
UMLS:C0241240 "Tall stature" [Orphanet:53250]
UMLS:C0017547 "Gigantism" [Orphanet:53250]
Is a (Direct Parents):
MedDRA Physical examination procedures and organ system status
HPO         Abnormality of body height
Orphanet Build/stature/longevity anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Abnormality of body height(HPO:0000002)
             Tall stature(HPO:0000098)
MedDRA:
Investigations(MedDRA:10022891)
    Physical examination and organ system status topics(MedDRA:10071940)
       Physical examination procedures and organ system status(MedDRA:10071941)
          Tall stature(HPO:0000098)
Database Frequency: 74 / 7739
Resource:

All diseases associated with this symptom:

17p13.3 microduplication syndrome (Orphanet:217385)
17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
46,XY SEX REVERSAL 1 (OMIM:400044)
46,XY complete gonadal dysgenesis (Orphanet:242)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA (OMIM:102100)
Acrocallosal syndrome (Orphanet:36)
Acromegaly (Orphanet:963)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Atkin-Flaitz syndrome (Orphanet:1193)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Beckwith-Wiedemann syndrome (Orphanet:116)
CLAPO syndrome (Orphanet:168984)
CLARK-BARAITSER SYNDROME (OMIM:300602)
Camptodactyly - tall stature - scoliosis - hearing loss (Orphanet:85164)
Cerebral gigantism - jaw cysts (Orphanet:2081)
Complete androgen insensitivity syndrome (Orphanet:99429)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Diabetic embryopathy (Orphanet:1926)
Distal trisomy 15q (Orphanet:1707)
Dysmorphism - cleft palate - loose skin (Orphanet:1779)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Familial glucocorticoid deficiency (Orphanet:361)
GIACHETI SYNDROME (OMIM:612917)
GLUCOCORTICOID DEFICIENCY 1 (OMIM:202200)
Gamma-aminobutyric acid transaminase deficiency (Orphanet:2066)
Gorlin syndrome (Orphanet:377)
Hydrocephaly - tall stature - joint laxity (Orphanet:2181)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit, X-linked - precocious puberty - obesity (Orphanet:85318)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Klippel-Trénaunay syndrome (Orphanet:90308)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lhermitte-Duclos disease (Orphanet:65285)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MGAT2-CDG (Orphanet:79329)
MOMO syndrome (Orphanet:2563)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Marshall-Smith syndrome (Orphanet:561)
McCune-Albright syndrome (Orphanet:562)
Microcephaly - glomerulonephritis - marfanoid habitus (Orphanet:2172)
Monosomy 22q13 (Orphanet:48652)
Monosomy 9q22.3 (Orphanet:77301)
Mosaic trisomy 8 (Orphanet:96061)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Neurofibromatosis type 1 (Orphanet:636)
PREMATURE OVARIAN FAILURE 2B (OMIM:300604)
Perlman syndrome (Orphanet:2849)
Progressive non-infectious anterior vertebral fusion (Orphanet:2062)
Proteus syndrome (Orphanet:744)
RIENHOFF SYNDROME (OMIM:615582)
Sclerosteosis (Orphanet:3152)
Sillence syndrome (Orphanet:3168)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Sotos syndrome (Orphanet:821)
Summitt syndrome (Orphanet:3210)
TMCO1 defect syndrome (Orphanet:228407)
Testotoxicosis (Orphanet:3000)
Trisomy X (Orphanet:3375)
Weaver syndrome (Orphanet:3447)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Zunich-Kaye syndrome (Orphanet:3474)