Abnormal dermatoglyphics

Symptom Information:

Symptom ID: HPO:0007477
Dermatoglyphic abnormalities [HPO:0007477]
Dermatoglyphics anomaly [Orphanet:20220]
Abnormal dermatoglyphics [OMIM:Abnormal dermatoglyphics]
Dermatoglyphic abnormalities [OMIM:Dermatoglyphic abnormalities]
Abnormal dermatoglyphics [Orphanet:20220]
Dermatoglyphic anomaly [MedDRA:10061455]
Cross references:
HPO:0001018 "Abnormal palmar dermatoglyphics" [Orphanet:20220]
Orphanet:20220 "Abnormal dermatoglyphics" [Orphanet:20220]
OMIM: "Abnormal dermatoglyphics" [OMIM:Abnormal dermatoglyphics]
OMIM: "Dermatoglyphic abnormalities" [OMIM:Dermatoglyphic abnormalities]
Is a (Direct Parents):
MedDRA Dermal and epidermal conditions NEC
HPO         Regional abnormality of skin
Orphanet Abnormality of the hand
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Regional abnormality of skin(HPO:0011356)
                Abnormal dermatoglyphics(HPO:0007477)
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Dermal and epidermal conditions NEC(MedDRA:10012424)
          Abnormal dermatoglyphics(HPO:0007477)
Database Frequency: 72 / 7739

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Absence of fingerprints - congenital milia (Orphanet:1658)
Achalasia - microcephaly (Orphanet:929)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Böök syndrome (Orphanet:1262)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cenani-Lenz syndrome (Orphanet:3258)
Cerebro-reno-digital syndrome (Orphanet:1396)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Cooper-Jabs syndrome (Orphanet:1488)
Costello syndrome (Orphanet:3071)
Crossed polysyndactyly (Orphanet:2935)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Dermo-odonto dysplasia (Orphanet:1660)
Distal trisomy 18q (Orphanet:1716)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Extrasystoles - short stature - hyperpigmentation - microcephaly (Orphanet:1964)
Fetal alcohol syndrome (Orphanet:1915)
Fetal hydantoin syndrome (Orphanet:1912)
Hand-foot-genital syndrome (Orphanet:2438)
Heart defect - round face - congenital developmental delay (Orphanet:1355)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hypertryptophanemia (Orphanet:2224)
IVIC syndrome (Orphanet:2307)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Miles-Carpenter type (Orphanet:85283)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
Kabuki syndrome (Orphanet:2322)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lichstenstein syndrome (Orphanet:2390)
Low birth weight - dwarfism - dysgammaglobulinemia (Orphanet:2621)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Monosomy 13q14 (Orphanet:1587)
Monosomy 9p (Orphanet:261112)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
Noonan syndrome (Orphanet:648)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Otofaciocervical syndrome (Orphanet:2792)
Poland syndrome (Orphanet:2911)
Postaxial acrofacial dysostosis (Orphanet:246)
Progeroid syndrome, Petty type (Orphanet:2963)
Qazi-Markouizos syndrome (Orphanet:3010)
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema (Orphanet:2252)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Synostosis - microcephaly - scoliosis (Orphanet:3268)
Teebi-Shaltout syndrome (Orphanet:3291)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Thoraco-abdominal enteric duplication (Orphanet:1759)
Toluene embryopathy (Orphanet:1920)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trigonocephaly - broad thumbs (Orphanet:3365)
Trisomy 13 (Orphanet:3378)
Trisomy 18 (Orphanet:3380)
Trisomy 9p (Orphanet:236)
Turner syndrome (Orphanet:881)
Williams syndrome (Orphanet:904)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)