Small nail

Symptom Information:

Symptom ID: HPO:0001792
Synonyms:
Hypoplastic nail [HPO:0001792]
Hypoplastic nails [HPO:0001792]
Nail hypoplasia [HPO:0001792]
Small nails [HPO:0001792]
Small nail of foot [Orphanet:25350]
Small nail of hand [Orphanet:25100]
Hypoplastic nails [OMIM:Hypoplastic nails]
Nail hypoplasia [OMIM:Nail hypoplasia]
Small nails [OMIM:Small nails]
Absent/small toenails/anonychia of feet [Orphanet:25350]
Absent/small fingernails/anonychia of hands [Orphanet:25100]
Hypoplastic nail (thumbs and halluces) [OMIM:Hypoplastic nail (thumbs and halluces)]
Hypoplastic nails (5th toes) [OMIM:Hypoplastic nails (5th toes)]
Hypoplastic nails (in some patients) [OMIM:Hypoplastic nails (in some patients)]
Nail hypoplasia (some) [OMIM:Nail hypoplasia (some)]
Quality:
Cross references:
Orphanet:25350 "Absent/small toenails/anonychia of feet" [Orphanet:25350]
Orphanet:25100 "Absent/small fingernails/anonychia of hands" [Orphanet:25100]
OMIM: "Hypoplastic nails" [OMIM:Hypoplastic nails]
OMIM: "Nail hypoplasia" [OMIM:Nail hypoplasia]
OMIM: "Small nails" [OMIM:Small nails]
OMIM: "Hypoplastic nail (thumbs and halluces)" [OMIM:Hypoplastic nail (thumbs and halluces)]
OMIM: "Hypoplastic nails (5th toes)" [OMIM:Hypoplastic nails (5th toes)]
OMIM: "Hypoplastic nails (in some patients)" [OMIM:Hypoplastic nails (in some patients)]
OMIM: "Nail hypoplasia (some)" [OMIM:Nail hypoplasia (some)]
Is a (Direct Parents):
Orphanet Abnormality of the toenails
Orphanet Abnormality of the fingernails
HPO         Aplasia/Hypoplasia of the nails
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the nail(HPO:0001597)
                Aplasia/Hypoplasia of the nails(HPO:0008386)
                   Small nail(HPO:0001792)
MedDRA:
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
ALG3-CDG (Orphanet:79321)
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib (OMIM:615631)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Adams-Oliver syndrome (Orphanet:974)
BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION (OMIM:613627)
Bartsocas-Papas syndrome (Orphanet:1234)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Deafness - onychodystrophy (Orphanet:3231)
Deafness - onychodystrophy, autosomal dominant (Orphanet:79499)
Distal monosomy 10q (Orphanet:96148)
Distal symphalangism (Orphanet:3248)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
FACIOTHORACOGENITAL SYNDROME (OMIM:227320)
Faciocardiorenal syndrome (Orphanet:1973)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Fryns syndrome (Orphanet:2059)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
Galloway-Mowat syndrome (Orphanet:2065)
Geleophysic dysplasia (Orphanet:2623)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypodontia - dysplasia of nails (Orphanet:2228)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 (OMIM:242100)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Odontotrichomelic syndrome (Orphanet:2723)
Palmoplantar keratoderma-sclerodactyly syndrome (Orphanet:384)
Polysyndactyly - cardiac malformation (Orphanet:2934)
RAPP-HODGKIN SYNDROME (OMIM:129400)
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH (OMIM:606895)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Self-healing collodion baby (Orphanet:281122)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Sotos syndrome (Orphanet:821)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 (OMIM:234050)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
Zechi-Ceide syndrome (Orphanet:217017)
Zimmermann-Laband syndrome (Orphanet:3473)