Micropenis

Symptom Information:

Symptom ID: HPO:0000054
Synonyms:
Microphallus [HPO:0000054]
Short penis [HPO:0000054]
Small penis [HPO:0000054]
Congenital hypoplasia of penis (disorder) [Orphanet:39240]
Small penis (finding) [Orphanet:39240]
Small penis [Orphanet:39240]
Congenital hypoplasia of penis [Orphanet:39240]
Micropenis [OMIM:Micropenis]
Microphallus [OMIM:Microphallus]
Short penis [OMIM:Short penis]
Small penis [OMIM:Small penis]
Micropenis/small penis/agenesis [Orphanet:39240]
Small penis (100%) [OMIM:Small penis (100%)]
Small penis (84%) [OMIM:Small penis (84%)]
Small penis (in some patients) [OMIM:Small penis (in some patients)]
Small penis (rare) [OMIM:Small penis (rare)]
Micropenis [MedDRA:10071706]
Quality:
Cross references:
Orphanet:39240 "Micropenis/small penis/agenesis" [Orphanet:39240]
OMIM: "Micropenis" [OMIM:Micropenis]
OMIM: "Microphallus" [OMIM:Microphallus]
OMIM: "Short penis" [OMIM:Short penis]
OMIM: "Small penis" [OMIM:Small penis]
OMIM: "Small penis (100%)" [OMIM:Small penis (100%)]
OMIM: "Small penis (84%)" [OMIM:Small penis (84%)]
OMIM: "Small penis (in some patients)" [OMIM:Small penis (in some patients)]
OMIM: "Small penis (rare)" [OMIM:Small penis (rare)]
UMLS:C0266435 "Micropenis" [HPO:0000054]
UMLS:C0240701 "Small penis" [Orphanet:39240]
UMLS:C0266435 "Congenital hypoplasia of penis" [Orphanet:39240]
Is a (Direct Parents):
Orphanet Abnormality of the penis
MedDRA Penile disorders NEC (excl erection and ejaculation)
HPO         Hypoplasia of penis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
             Abnormal genital system morphology(HPO:0012243)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the penis(HPO:0000036)
                         Hypoplasia of penis(HPO:0008736)
                            Micropenis(HPO:0000054)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
                            Micropenis(HPO:0000054)
                Abnormal external genitalia(HPO:0000811)
                   External genital hypoplasia(HPO:0003241)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
                            Micropenis(HPO:0000054)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the penis(HPO:0000036)
                         Hypoplasia of penis(HPO:0008736)
                            Micropenis(HPO:0000054)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
                            Micropenis(HPO:0000054)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Penile and scrotal disorders (excl infections and inflammations)(MedDRA:10013355)
       Penile disorders NEC (excl erection and ejaculation)(MedDRA:10034304)
          Micropenis(HPO:0000054)
Database Frequency: 257 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17p13.3 microduplication syndrome (Orphanet:217385)
1p36 deletion syndrome (Orphanet:1606)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q23.1 microdeletion syndrome (Orphanet:228402)
3C syndrome (Orphanet:7)
3MC SYNDROME 3 (OMIM:248340)
3q13 microdeletion syndrome (Orphanet:1621)
46,XX ovotesticular disorder of sex development (Orphanet:2138)
46,XX testicular disorder of sex development (Orphanet:393)
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency (Orphanet:753)
46,XY partial gonadal dysgenesis (Orphanet:251510)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
8p11.2 deletion syndrome (Orphanet:251066)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Ablepharon macrostomia syndrome (Orphanet:920)
Acro-cardio-facial syndrome (Orphanet:2008)
Acrocallosal syndrome (Orphanet:36)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Alopecia - intellectual deficit - hypergonadotropic hypogonadism (Orphanet:1014)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant omodysplasia (Orphanet:93328)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive amelia (Orphanet:1027)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Baraitser-Winter syndrome (Orphanet:2995)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 8 (OMIM:615985)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Bladder exstrophy (Orphanet:93930)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Brachydactyly - nystagmus - cerebellar ataxia (Orphanet:1246)
Brachydactyly type B (Orphanet:93383)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CARPENTER SYNDROME 2 (OMIM:614976)
CEREBROOCULOFACIOSKELETAL SYNDROME 2 (OMIM:610756)
CHARGE syndrome (Orphanet:138)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
CULLER-JONES SYNDROME (OMIM:615849)
Cabezas syndrome (Orphanet:85293)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Carpenter-Waziri syndrome (Orphanet:93973)
Cataract - intellectual deficit - anal atresia - urinary defects (Orphanet:1381)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Caudal appendage - deafness (Orphanet:1123)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Cloacal exstrophy (Orphanet:93929)
Cockayne syndrome (Orphanet:191)
Congenital osteogenesis imperfecta - microcephaly - cataracts (Orphanet:2772)
Cornelia de Lange syndrome (Orphanet:199)
Crandall syndrome (Orphanet:202)
Crane-Heise syndrome (Orphanet:1512)
Craniofacial-ulnar-renal syndrome (Orphanet:293843)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Crossed polysyndactyly (Orphanet:2935)
Currarino triad (Orphanet:1552)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal monosomy 10p (Orphanet:1580)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 15q (Orphanet:1596)
Distal monosomy 7q36 (Orphanet:1636)
Distal trisomy 18q (Orphanet:1716)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
Emanuel syndrome (Orphanet:96170)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Endomyocardial fibroelastosis (Orphanet:2022)
Exstrophy-epispadias complex (Orphanet:322)
FANCONI ANEMIA, COMPLEMENTATION GROUP L (OMIM:614083)
Familial adrenal hypoplasia with absent pituitary luteinizing hormone (Orphanet:95700)
Femoral-facial syndrome (Orphanet:1988)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Floating-Harbor syndrome (Orphanet:2044)
Fraser syndrome (Orphanet:2052)
Gemignani syndrome (Orphanet:2074)
Genitopatellar syndrome (Orphanet:85201)
Growth hormone insensitivity syndrome (Orphanet:181393)
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION (OMIM:613870)
HOLOPROSENCEPHALY 1 (OMIM:236100)
HOLOPROSENCEPHALY 9 (OMIM:610829)
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS (OMIM:610680)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED (OMIM:241100)
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA (OMIM:308700)
HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA (OMIM:614840)
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA (OMIM:614841)
HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA (OMIM:614880)
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA (OMIM:614897)
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA (OMIM:616030)
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA (OMIM:228300)
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA (OMIM:244200)
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA (OMIM:610628)
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA (OMIM:614837)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Hand-foot-genital syndrome (Orphanet:2438)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Holmes-Gang syndrome (Orphanet:93970)
Holoprosencephaly (Orphanet:2162)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hydrocephalus - obesity - hypogonadism (Orphanet:2183)
Hypogonadotropic hypogonadism - frontoparietal alopecia (Orphanet:2230)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
IMAGe syndrome (Orphanet:85173)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Johanson-Blizzard syndrome (Orphanet:2315)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 2 (OMIM:608091)
Juberg-Marsidi syndrome (Orphanet:93972)
KABUKI SYNDROME 1 (OMIM:147920)
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA (OMIM:308750)
Kabuki syndrome (Orphanet:2322)
Kallmann syndrome (Orphanet:478)
Kallmann syndrome - heart disease (Orphanet:2326)
Kapur-Toriello syndrome (Orphanet:2328)
Kenny-Caffey syndrome (Orphanet:2333)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
LEOPARD SYNDROME 1 (OMIM:151100)
LIG4 syndrome (Orphanet:99812)
Laron syndrome (Orphanet:633)
Lathosterolosis (Orphanet:46059)
Laurence-Moon syndrome (Orphanet:2377)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Lissencephaly type 1 due to doublecortin gene mutation (Orphanet:2148)
MEHMO syndrome (Orphanet:85282)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MEIER-GORLIN SYNDROME 5 (OMIM:613805)
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENISSYNDROME (OMIM:610156)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MOVED TO 614732 (OMIM:300290)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Marden-Walker syndrome (Orphanet:2461)
Maternal hyperthermia induced birth defects (Orphanet:2216)
Meacham syndrome (Orphanet:3097)
Micro syndrome (Orphanet:2510)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Mikati-Najjar-Sahli syndrome (Orphanet:2558)
Moebius syndrome (Orphanet:570)
Monosomy 18p (Orphanet:1598)
Monosomy 18q (Orphanet:1600)
Monosomy 9p (Orphanet:261112)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 9 (Orphanet:99776)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome with multiple lentigines (Orphanet:500)
Normosmic congenital hypogonadotropic hypogonadism (Orphanet:432)
OROFACIODIGITAL SYNDROME XIV (OMIM:615948)
Obesity due to congenital leptin deficiency (Orphanet:66628)
Omodysplasia (Orphanet:2733)
Osteocraniostenosis (Orphanet:2763)
PELVIS syndrome (Orphanet:83628)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pallister-Hall syndrome (Orphanet:672)
Partial androgen insensitivity syndrome (Orphanet:90797)
Perlman syndrome (Orphanet:2849)
Phocomelia, Schinzel type (Orphanet:2879)
Pierson syndrome (Orphanet:2670)
Pitt-Hopkins syndrome (Orphanet:2896)
Pituitary stalk interruption syndrome (Orphanet:95496)
Pontocerebellar hypoplasia type 7 (Orphanet:284339)
Postaxial acrofacial dysostosis (Orphanet:246)
Potocki-Shaffer syndrome (Orphanet:52022)
Prader-Willi syndrome (Orphanet:739)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 (OMIM:616331)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Retinitis pigmentosa (Orphanet:791)
Retinohepatoendocrinologic syndrome (Orphanet:3087)
Rudiger syndrome (Orphanet:3118)
SCARF syndrome (Orphanet:3134)
SCHAAF-YANG SYNDROME (OMIM:615547)
SENER SYNDROME (OMIM:606156)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB (OMIM:615087)
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION (OMIM:612447)
STT3B-CDG (Orphanet:370924)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Septo-optic dysplasia (Orphanet:3157)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Summitt syndrome (Orphanet:3210)
Syndromic X-linked intellectual deficit 7 (Orphanet:85274)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Syndromic microphthalmia type 5 (Orphanet:178364)
TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE (OMIM:615542)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Testicular regression syndrome (Orphanet:983)
Toriello-Carey syndrome (Orphanet:3338)
Townes-Brocks syndrome (Orphanet:857)
Treacher-Collins syndrome (Orphanet:861)
Triploidy (Orphanet:3376)
Trisomy 17p (Orphanet:261290)
Trisomy 5p (Orphanet:1742)
Trisomy 8q (Orphanet:1752)
Ulnar-mammary syndrome (Orphanet:3138)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
VACTERL/VATER association (Orphanet:887)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Von Voss-Cherstvoy syndrome (Orphanet:3439)
WARBURG MICRO SYNDROME 2 (OMIM:614225)
WARBURG MICRO SYNDROME 3 (OMIM:614222)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
Walker-Warburg syndrome (Orphanet:899)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Wilson-Turner syndrome (Orphanet:3459)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Yunis-Varon syndrome (Orphanet:3472)